CN1533267A

CN1533267A - Cosmetic compositions

Info

Publication number: CN1533267A
Application number: CNA018135099A
Authority: CN
Inventors: J��M��ɣ�ƶ�; J·M·桑科尔; M·L·瓦特
Original assignee: Procter and Gamble Ltd
Current assignee: Procter and Gamble Ltd
Priority date: 2000-07-10
Filing date: 2001-07-09
Publication date: 2004-09-29
Anticipated expiration: 2021-07-09
Also published as: ES2316456T3; WO2002003951A3; AU7192801A; AU2001271928C1; KR20030045011A; US20020028184A1; US6524598B2; ATE414505T1; EP1355624B1; DE60136650D1; WO2002003951A2; MXPA03000262A; AU2001271928B2; KR100532835B1; CA2412961C; CZ200384A3; JP2004502715A; EP1355624A2; JP2006193531A; CN1235564C

Abstract

The invention relates to cosmetic compositions comprising a combination of non-emulsifying and emulsifying crosslinked siloxane elastomers.

Description

Cosmetic composition

The cross reference of related application

The application requires the interests of No. 60/217,14, the U.S. Provisional Patent Application of on July 10th, 2000 application.

Invention field

The present invention relates to comprise non-emulsifying and emulsifying cross-linked siloxane elastomer composite face-painting product compositions.

Background of invention

Emollient comprises organic ester and Hydrocarbon, and especially mineral fat has very long medical science to use as skin conditioning agent.As the selection of moistening composition, these materials are only second to water.They are mainly as the occlusive barrier layer.The outer water content of human skin cutin is a kind of governing factor of dry skin symptom.When horny layer contains the water of q.s, in the time of in 10% to 20% scope, skin is softish.Yet when moisture drops to when being lower than 10%, horny layer becomes fragile and coarse and shows through regular meeting and peels off and break.

Horny layer obtains self moisture by diffusion from the epidermis deep layer, perhaps obtains moisture by directly contacting with water.Diffusion process is controlled jointly by water content in the skin and Concentraton gradient.In very exsiccant environment, it is very important and often surpass the speed of diffusion and replacement that the moisture loss of skin outer layer just becomes.Occlusive or half occlusive barrier substance are coated on skin surface can play the effect of moisture loss to environment that stop.It also can make skin surface rehydration by diffusion mechanism.

Though the effectively economic skin conditioning agent of many kinds is arranged, yet they always suffer some unfavorable shortcoming.

Usually emollient is carried with the form of water-in-oil emulsion.Reaching critical preparation balance between oil phase and water makes it can have abundant degree to guarantee that long-term storage stability is very difficult.The one side of critical balance is interior phase volume.Must obtain critical size enlarge to greatest extent the chemistry and physical interaction in order to the creation and stabilisation systems.If critical size does not have suitably balance, the viscosity variation will take place product and final the generation is separated.Common optimum volume is quite big, and this will limit foreign minister's volume size, and brings the disadvantageous slow fracture properties of a kind of retardance of system.The restriction of critical interior phase volume can reduce functional and increase disadvantageous sense quality.

High-caliber relatively water base moistening composition (for example glycerol) need carry in new system.

Therefore, one aspect of the present invention provides the cosmetic composition that improves the skin tactile characteristics.

Even another aspect of the present invention provides the composition for processing skin that has stability under freeze to being separated.

Of the present invention providing on the other hand again is coated on the composition for processing skin that skin obtains smooth fluent friction seeping for the first time.

These and other aspects of the present invention are more readily understood in the consideration result of following summary and detailed description.

Invention is summed up

The present invention relates to cosmetic composition, comprise:

(i) non-emulsifying cross-linked siloxane elastomer, content are from about 0.1% to about 15%, and its mean diameter is less than 20 microns.

(ii) emulsifying cross-linked siloxane elastomer, content from about 0.1% to about 15%.

The (iii) solvent of crosslinked siloxane elastomer, content from about 10% to about 80%.

(iv) selectively, skin conditioning agent, content from about 0% to about 50%; With

(v) water, content from about 0% to about 95%.

The invention also discloses cosmetic composition, contain:

(i) about 0.1% to the crosslinked siloxane elastomer of about 15% average grain granularity less than 20 microns;

(ii) 10 to 80% solvents that are used for crosslinked siloxane elastomer;

(iii) not necessarily, 0 to 50% skin conditioning agent; With

(iv) not necessarily, greater than about 0 to about 95% water,

Wherein compositions contains the air at least about 1%.

Detailed Description Of The Invention

Among the present invention, term " cosmetics " comprises cosmetics, foundation cream and skin-protection product.Term " cosmetics " refers to stay at face the product of color, comprises foundation cream, black and brown product, that is, mascara is covered flaw agent, informer, eyebrow coloured silk, eye shadow, kermes, lip gloss, powder, solid emulsion moulding powder or the like.Skin-protection product is to be used for handling or the product of nursing, moistening, improvement or cleaning skin.The product of phrase " skin-protection product " indication includes, but is not limited to binding agent, binder type product, toothpaste, anhydrous occlusion humidizer, antiperspirant, deodorizer, personal cleansing product, detergent, fabric sofetening towel, the occlusion administration patch, nial polish, powder, brocade, wiping cloth, hair conditioner-anhydrous type, shaving cream or the like.Term " excess water " refers to be deposited on the body fluid that do not expect and/or unsound content on the human body skin.Term " foundation cream " refers to the liquid that cosmetics company produces or introduces, cream, and mousse, muffin is pressed into powder, covers similar products such as flaw agent, is used for smoothing the whole color and luster of skin.Make foundation cream and be to better at humidification and/or increase on the oily skin and work.

Term " environmental condition " refers to be in the ambient conditions under an about atmospheric pressure, about 50% relative humidity and about 25 ℃ in the present invention, unless otherwise prescribed.

That term " causes stream power value " and refers to astaticism and refer to the mobile starting force of opposing under the stress of using; It is to adopt the Haake controlled stress flow graph RS150 with 35 millimeters/4 degree circular cones and dish to record.

Among the present invention, term " contains " and means compositions and can contain other composition, and these compositions and compositions are compatible and preferably do not destroy compositions of the present invention basically.This term comprise term " by ... form " and " basically by ... composition ".

Except as otherwise noted, among the present invention used all percents and ratio all in the weight of total compositions.Except as otherwise noted, all wt percentage number average is based on the weight of active matter.All measurements are all carried out under 25 ℃, except as otherwise noted.

The crosslinked polysiloxane elastomer

One of solvent of the present invention is crosslinked organopolysiloxane elastomer.Kind for the curable organopolysiloxane composition that can be used as the elastomeric initiation material of cross-lined organic polyorganosiloxane does not have clear and definite restriction.The example of this respect is the solidified organopolysiloxane composition of additive reaction, and wherein the additive reaction between diorganopolysiloxanecompositions by containing SiH under the platinum catalysis and organopolysiloxane with silicon bonding ethylene base is solidified; Condensation cured organopolysiloxane composition wherein solidifies by hydroxy-end capped diorganopolysiloxanecompositions and the dehydrogenation reaction that contains between the diorganopolysiloxanecompositions of SiH in the presence of organo-tin compound; Condensation cured organopolysiloxane composition wherein solidifies by the condensation reaction between hydroxy-end capped diorganopolysiloxanecompositions and the hydrolyzable organosilan (this condensation reaction can dehydration, dealcoholysis, take off oxime, take off amine, deacylated tRNA amine, decarboxylation and take off reactive ketone as an example) in the presence of the chemical compound of organotin or titanate esters; Peroxide cure organopolysiloxane composition, wherein heat cure in the presence of organic peroxide catalyst; And by organopolysiloxane composition as the high-energy radiation solidification of gamma-radiation, ultraviolet or electron beam.

The additive reaction curing organopolysiloxane composition because of its rapidly solidification rate and solidify in good homogeneous be preferred.Particularly preferred additive reaction curing organopolysiloxane composition is prepared by following material:

(A) in each molecule, has the organopolysiloxane of at least 2 low-grade alkenyls;

(B) in each molecule, has the organopolysiloxane of at least 2 silicon bonded hydrogen atom; With

(C) catalyst of platinum type.

About above-mentioned substance, composition (A) is the basis of the organopolysiloxane that generates silicone elastomer, by under the catalysis of composition (C), the additive reaction of this composition and composition (B) is cured.This composition (A) contains the low-grade alkenyl of at least 2 silicon bondings in must per molecule; Owing to can not form network structure, can not obtain the product of good solidification when being less than two low-grade alkenyls.The example of this low-grade alkenyl has vinyl, pi-allyl and acrylic.Though low-grade alkenyl can be present in any position in the molecule, it is present in molecular end is preferred.The molecular structure of this composition can be straight chain, the ring-type or netted of straight chain, branching, but slightly the straight chain of branching is preferred.The molecular weight of this composition does not have clear and definite restriction, thereby its viscosity can be from low-viscosity (mobile) liquid to very full-bodied colloid.In order to make the cured article that obtains is the form of rubber elastomer, and the viscosity under 25 degrees centigrade is at least 100 centistokes for preferred.The example of these organopolysiloxanes has the ethylene methacrylic radical siloxane, ethylene methacrylic radical siloxane-dimethylsiloxane copolymer, dimethylvinylsiloxy end-blocking dimethyl polysiloxane, dimethylvinylsiloxy end-blocking dimethyl siloxane-methyl phenyl siloxane copolymer, dimethylvinylsiloxy end-blocking dimethyl siloxane-diphenyl siloxane-methyl ethylene silicone copolymers, trimethylsiloxy end-blocking dimethyl siloxane-methyl ethylene silicone copolymers, trimethylsiloxy end-blocking dimethyl siloxane-methyl phenyl siloxane-methyl ethylene silicone copolymers, dimethylvinylsiloxy end-blocking methyl (3,3, the 3-trifluoro propyl) polysiloxanes and dimethylvinylsiloxy end-blocking dimethyl siloxane-methyl (3,3 ,-trifluoro propyl) silicone copolymers.

The organopolysiloxane of composition (B) for having at least 2 silicon bonded hydrogen atom in the per molecule, and be the cross-linking agent of composition (A).Be cured by the silicon bonded hydrogen atom under the catalysis of composition (C), in this composition and the additive reaction of the low-grade alkenyl in the composition (A).This composition (B) must contain at least 2 silicon bonded hydrogen atom in the per molecule, to play cross-linking agent.In addition, the summation of the number of the silicon bonded hydrogen atom in the per molecule of the number of the thiazolinyl in the per molecule of composition (A) and composition (B) is at least 5.Because network structure can not form basically, should avoid being lower than 5 value.

Molecular structure for this composition does not have clear and definite restriction, and it can be straight chain, contains any of the straight chain of side chain, ring-type or the like.The molecular weight of this composition does not have clear and definite restriction, but 25 degrees centigrade of viscosity down are that 1 to 50,000 centistoke be preferably, to obtain and the good compatibility of composition (A).Preferably the addition of this composition be make mol ratio between the total amount of all low-grade alkenyls in the total amount of the silicon bonded hydrogen atom in this composition and the composition (A) in (1.5: 1) in the scope of (20: 1).When this mol ratio is lower than 0.5: 1, be difficult to obtain good curing performance.When surpassing (20: 1), when the product that is heating and curing, hardness increases to high-caliber trend.In addition, for as the purpose strengthened replenish and add when containing the organopolysiloxane of a large amount of thiazolinyls, preferably replenish this amount that contains the composition of SiH that adds and can offset these thiazolinyls.The concrete example of this composition has trimethylsiloxy end-blocking methylhydrogenpolysi,oxane, trimethylsiloxy end-blocking dimethyl siloxane-methylhydrogensiloxacopolymer copolymer and dimethyl siloxane-methyl hydrogen-siloxanes cyclocopolymer.

Composition (C) is the catalyst of the additive reaction of silicon bonded hydrogen atom and thiazolinyl, concrete example has chloroplatinic acid, it is not necessarily aging to be dissolved in alcohol or ketone and this solution, the platinum of chloroplatinic acid-alkene complex, chloroplatinic acid-alkenyl siloxane complex, chloroplatinic acid-diketone complex, platinum black and carrier supported.

Add the total amount of (B) as the composition (A) of suitably per 1,000,000 weight portion of platinum type metal, preferably with 0.1 to 1,000 weight portion, more preferably add this composition with 1 to 100 weight portion.Can be as alkyl with other organic group of silicon bonding in the organopolysiloxane on the basis that forms the foregoing curable organopolysiloxane composition, as methyl, ethyl, propyl group, butyl and octyl group; Substituted alkyl is as 2-phenethyl, 2-phenylpropyl and 3,3,3-trifluoro propyl; Aryl is as phenyl, tolyl and xylyl; Substituted aryl is as phenethyl; And by the univalence hydrocarbyl that replaces as epoxy radicals, carboxylic acid ester groups, sulfydryl or the like.

The embodiment of preparation organopolysiloxane elastomer powder is as follows: in the presence of surfactant (nonionic, anion, cation or amphoteric) that above-mentioned organopolysiloxane composition (addition curing, condensation cured or peroxide cure) and water is mixed, after in homo-mixer, colloid mill, homogenizer, propeller mixer or the like, mixing evenly, solidify by being discharged in the hot water (temperature is at least 50 degrees centigrade), dry then; By directly being ejected into, it makes organopolysiloxane composition (addition-curable, condensation cured or peroxide cure) curing in thermal current; Obtain powder by it is sprayed the organopolysiloxane composition that solidifies radiation-hardenable under high-energy radiation; With organopolysiloxane composition (addition-curable, condensation cured, peroxide cure) but or the solidified organopolysiloxane composition of high energy solidify, the latter passes through high-energy radiation solidification, with known pulverizer such as ball mill, atomizer, kneading machine, roll mill or the like product is ground then, thereby form powder.Suitable organopolysiloxane elastomer powder comprises vinyl-dimethyl based polysiloxane/methyl polysiloxane silsesquioxane (silesquioxane) cross linked polymer, KSP-100, KSP-101, KSP-102, KSP-103, KSP-104, KSP-105 as Shin-Etsu, comprise the hybrid silicone powder of fluoro-alkyl group such as the KSP-200 of Shin-Etsu, comprise the hybrid silicone powder of phenyl group such as the KSP-300 of Shin-Etsu; The DC 9506 of Dow Corning.

Preferably, organopolysiloxane composition is dimethyl polysiloxane/vinyl-dimethyl polysiloxanes cross linked polymer.This type of dimethyl polysiloxane/vinyl-dimethyl polysiloxanes cross linked polymer can be provided by how tame supplier, comprise Dow Corning (DC 9040 and DC 9041), General Electric (SFE 839), Shin Etsu (KSG-15,16,18[dimethyl polysiloxane/phenyl vinyl dimethicone cross linked polymer]) and Grant Industries (Gransil ^TMSeries material) and the dodecyl dimethicone/vinyl dimethicone crosspolymers (for example KSG-31, KSG-32, KSG-41, KSG-42, KSG-43 and KSG-44) that provides of Shin Etsu.Cross-lined organic polyorganosiloxane elastomer used in the present invention and manufacturing process thereof have further instruction in following patent: people's such as mandate on November 13 nineteen ninety Sakuta United States Patent (USP) 4,970,252; People's such as mandate on June 2nd, 1998 Kilgour United States Patent (USP) 5,760,116; Authorized Schulz, people's such as Jr United States Patent (USP) 5,654,362 on August 5th, 1997; With Japanese patent application JP61-18708, transfer Pola KaseiKogyo KK, every patent completely is introduced in Insert Here by it.

Compositions of the present invention comprises emulsifying and the elastomeric combination of non-emulsification and cross linked organopolysiloxane.Term used herein " non-emulsifying " has defined and has not contained the unitary cross-lined organic polyorganosiloxane elastomer of polyoxyalkylene.Term used herein " emulsifying " is meant (as polyoxyethylene or polyoxypropylene) the unitary cross-lined organic polyorganosiloxane elastomer that has at least one polyoxyalkylene.Emulsification and cross linked organopolysiloxane elastomer can be especially from United States Patent (USP) 5,412,004 (mandate on May 2nd, 95), 5,837,793 (mandates on November 17th, 98) and 5, the cross linked polymer of introducing in 811,487 (JIUYUE was authorized on the 22nd in 98 years) is chosen, and all patents are quoted by its integral body and inserted herein.

Especially the emulsifying elastomer of Shi Yonging is by divinyl compound, particularly has a polyoxyalkylene modified elastomer that the reaction of the siloxane polymer of at least two free vinyl and the Si-H key on the polysiloxanes skeleton forms.Preferably, elastomer is the crosslinked dimethyl polysiloxane in Si-H site on the spherical MQ resin of molecule.

Non-emulsifying cross-linked organopolysiloxane of the present invention preferably can by have circulation or not with the circulation sonolator in, in the presence of the solvent of silicone elastomer, make it stand high shear (about 5,000psi) handle and further processing, handle 10 to 60 journeys.The sound spectrum that adopts Horiba LA-910 (describing below) to record shows that the compositions of gained has and is less than 20 microns, preferably is less than 10 microns (or about 10 microns), preferably is less than the non-emulsifying elastomer of the mean diameter of 5 microns (or about 5 microns)." particle diameter " of term elastomer used herein represented the elastomer particle diameter of its swelling state." expansion " used herein is meant that because it has absorbed solvated compounds, elastomer particles surpasses the extension of its normal size and shape.Preferably, 25 ℃ down by Brookfield LV viscometer (size 4 bars, 60rpm 15sec.) measure, and viscosity is lower than 20,000cps (or about 20,000cps), preferably be lower than approximately 15,000, more preferably from about 100-is about 10,000cps.

The emulsive cross-lined organic polyorganosiloxane elastomer that compositions comprised among the present invention, from about 0.1 to about 15%, best is from about 1% to about 10%, more preferably from about 3% to 8% based on its concentration of weight.

The non-emulsive cross-lined organic polyorganosiloxane elastomer that compositions comprised among the present invention, from about 0.1 to about 15%, best is from about 1% to about 10%, more preferably from about 3% to 8% based on its concentration of weight.

Be used for non-emulsifying and emulsifying solvent with crosslinked siloxane elastomer

Compositions of the present invention contains the foregoing elastomeric solvent of cross-lined organic polyorganosiloxane that is used for.Solvent when combining with cross-lined organic polyorganosiloxane elastomer particles of the present invention, plays a part to suspend and the swelling elastomer particles, so that the net or the substrate of elasticity, similar gels are provided.The solvent that is used for crosslinked siloxane elastomer is a liquid under environmental condition, and preferably has low viscosity, so that be provided at the improved spreadability on the skin.

The concentration of the solvent in the cosmetic composition of the present invention first and foremost changes with the type and the amount of used solvent and crosslinked siloxane elastomer.The preferred concentration of solvent be about 10wt% of compositions to about 90wt%, preferably about 20wt% is about 80wt% extremely, more preferably from about 30wt% about 70wt% extremely.

The solvent that is used for crosslinked siloxane elastomer contains one or more suitable liquid-carriers of using to the application on human skin local coating.These liquid-carriers can be organically, contain siloxanes or fluorine-containing, volatility or nonvolatile, polarity or nonpolar, and precondition is this liquid-carrier at about 28 ℃ to about 250 ℃, preferred about 28 to about 100, preferred about 28 formation solution or other homogeneous liquid or liquid dispersion liquid to about 78 ℃ of silicone elastomer concentration of selecting with selected crosslinked siloxane elastomer down.The solvent that is used for crosslinked siloxane elastomer, its solubility parameter are preferably about 3 to about 13 (cal/cm ³) ^0.5, more preferably from about 5 to about 11 (cal/cm ³) ^0.5, first-selected about 5 to about 9 (cai/cm ³) ^0.5The solubility parameter of liquid-carrier or other material and the method for measuring this parameter are known in the chemical field.About influence (the Solubility Effects in Product of visible C.D.Vaughan of the description of solubility parameter and assay method thereof “ Rong degree of separating to product, packing, infiltration and preservation, Package, Penetration andPreservation) " 103 cosmetics and toilet articles 47-69, in October, 1988; And C.D.Vaughan, " in cosmetic formulations, use solubility parameter (Using SolubilityParameters in Cosmetics Formulation) ", 36 J.Soc.Cosmetic Chemists319-333, in JIUYUE, 1988/October, these articles are incorporated herein by reference.

Solvent preferably includes volatility, non-polar oil; Non-volatile, relative polarity is oily; Non-volatile, non-polar oil and non-volatile paraffin oils; Below will be to doing more complete discussion separately.Term " non-volatile " refers in the present invention show that vapour pressure is no more than the material of about 0.2mmHg and/or refers to that boiling point is at least about 300 ℃ material under an atmospheric pressure under 25 ℃ of atmospheric pressure.Term " volatility " refers to not belong to as previously mentioned all materials of " non-volatile " in the present invention.Phrase " relative polarity " means in the present invention aspect solubility parameter and has more polarity than another kind of material; That is, solubility parameter is high more, and liquid is got over tool polarity.Term " nonpolar " generally means material to have and is lower than about 6.5 (cal/cm ³) ^0.5Solubility parameter.

1. nonpolar, ethereal oil

Nonpolar, ethereal oil tends to give very desirable aesthetic characteristic to compositions of the present invention.So, preferably use nonpolar, ethereal oil with quite high consumption.Nonpolar, the ethereal oil that are particularly suitable for the present invention's use are selected from silicone oil; Hydrocarbon and composition thereof.This nonpolar, ethereal oil is disclosed in, for example, " cosmetics, Science and Technology (Cosmetics, Science, and Technology) ", Vol.1,27-104, Balsam and Sagarin compile, and 1972.It can be saturated or undersaturated can be used for nonpolar, ethereal oil of the present invention, has the aliphatic compounds feature and is ring straight or branched or that contain alicyclic or aromatics.Example preferably nonpolar, volatile hydrocarbon (for example comprises polydecanes such as Fancol ID and isodecane, Permethyl-99A, Presperse Inc. produces) and C7-C8 to C12-C15 isoparaffin (as, Isopar series, Exxon Chemicals produces).Nonpolar, volatile liquid silicone oil has disclosed in US patent 4,781,917 (Luebbe etc., 1988.11.1 authorizes), and its integral body is incorporated herein by reference.In addition, Todd etc., " volatile siloxane fluid (Volatile SIlicone Fluids for Cosmetics) that is used for cosmetics ", cosmetics and toilet articles, relevant for the description of various volatile siloxane materials, its integral body is incorporated herein by reference among the 91:27-32 (1976).Particularly preferred volatile silicone oil is selected from the ring-type volatile siloxane, and it is corresponding to following formula:

Wherein n is about 3 to about 7; With the straight chain volatile siloxane, it is corresponding to following formula:

(CH ₃) ₃Si--O--[Si(CH ₃) ₂-O] _m--Si(CH ₃) ₃

Wherein m is about 1 to about 7.Viscosity under common 25 ℃ of the straight chain volatile siloxane is less than about 5 centistokes, and the viscosity under 25 ℃ of annular siloxane is less than about 10 centistokes.The example very preferably of volatile silicone oil comprises the annular dimethyl polysiloxane of different viscosities, for example, and Dow Corning 200, Dow Corning 244, Dow Corning 245, Dow Corning344 and Dow Corning 345, (Dow Corning company product); SF-1204 and SF-1202 siloxanes fluids (G.E.Silicones product), GE 7207 and 7158 (General Electric company product) and SWS-03314 (SWS Silicones company product).

2. relative polarity, nonvolatile oil

It is " relative polarity " that this nonvolatile oil is compared with above-mentioned nonpolar, ethereal oil.Therefore, this nonvolatile cosolvent than at least a nonpolar, volatility by having more polarity (that is, having higher solubility parameter).Relative polarity, the nonvolatile oil that can use in the present invention are disclosed in, for example, " cosmetics, Science and Technology (Cosmetics, Science, andTechnology) ", Vol.1,27-104, Balsam and Sagarin compile, and 1972; US patent 4,202,879 (Shelton, 1980.5.13 authorizes) and 4,816,261 (Luebbe etc., 1989.3.28 authorizes), all these equal integral body are incorporated herein by reference.Can be used for relative polarity of the present invention, nonvolatile oil is preferably selected from silicone oil; Hydrocarbon ils; Aliphatic alcohol; Fatty acid; The ester of monobasic and dicarboxylic acids and monobasic and dihydroxylic alcohols; Polyethylene glycol oxide; Polypropylene oxide; The mixture of the polyethylene glycol oxide of aliphatic alcohol and polypropylene oxide ether; And their mixture.Can be used for relative polarity of the present invention, nonvolatile cosolvent can be saturated or undersaturated, have the aliphatic compounds feature and be ring straight or branched or that contain alicyclic or aromatics.More preferably, relative polarity, non-volatile liquid cosolvent are selected from the aliphatic alcohol with about 12-26 carbon atom; Fatty acid with about 12-26 carbon atom; Monocarboxylic acid and ester with alcohol of about 14-30 carbon atom; Dicarboxylic acids and ester with alcohol of about 10-30 carbon atom; Polyhydric alcohol and ester with carboxylic acid of about 5-26 carbon atom; The mixture of the ethoxylated ether of the aliphatic alcohol of about 12-26 carbon atom, propoxylated ether and ethoxylation and propoxylated ether, and ethoxylation and propenoxylated degree are lower than about 50; And their mixture.More preferably degree of propoxylation is lower than the propoxylated ether of about 50 C14-C18 aliphatic alcohol, the ester of C2-C8 alcohol and C12-C26 carboxylic acid (ethyl myristate for example, isopropyl palmitate), C12-C26 alcohol and benzoic ester (for example Finetex provide Finsolv TN), the diester of C2-C8 alcohol and adipic acid, decanedioic acid and phthalic acid (for example, Dermol DIPS, diisopropyl adipate, n-butyl phthalate), the polyol ester of C6-C26 carboxylic acid (for example, the sad propylene glycol ester of two capric acid/two, the isostearic acid propylene glycol ester); And their mixture.The side chain aliphatic series aliphatic alcohol of more preferably about 12-26 carbon atom.More preferably different hexadecanol, octyl group decanol, octyldodecanol and undecyl pentadecanol; First-selected is octyldodecanol.Preferred aliphatic aliphatic alcohol is particularly suitable for regulating with volatile liquid silicone oil of the present invention coupling the average dissolubility of solvent.

3. nonpolar, nonvolatile oil

Except that the liquid of above-mentioned discussion, the solvent that is used for crosslinked siloxane elastomer can also not necessarily comprise non-volatile, non-polar oil.Typically non-volatile, non-polar emollient is disclosed in, for example, " cosmetics, Science and Technology (Cosmetics, Science, and Technology) ", Vol.1,27-104, Balsam and Sagarin compile, and 1972; US patent 4,202,879 (Shelton, 1980.5.13 authorizes) and 4,816,261 (Luebbe etc., 1989.3.28 authorizes).It all is incorporated herein by reference.Can be used for nonvolatile oil of the present invention is nonvolatile basically polysiloxanes, paraffin oils and composition thereof.Can be used for polysiloxanes of the present invention and be selected from poly-alkylsiloxane, poly-aryl siloxanes, polyoxyethylene alkyl aryl radical siloxane, polyether siloxane copolymer and composition thereof.The example comprises that the viscosity under 25 ℃ is about 1 polydimethylsiloxane to about 100,000 centistokes.The viscosity that wherein can be used for preferred non-volatile siloxane emollient of the present invention and be under 25 ℃ is about 2 polydimethylsiloxane to about 400 centistokes.This poly-alkylsiloxane comprises Viscasil series (sale of General Electric company) and Dow Corning 200 series (sale of Dow Corning company).The polyoxyethylene alkyl aryl radical siloxane comprises that the viscosity under 25 ℃ is about 15 PSIs to about 65 centistokes.It can, for example, obtain as the form of SF 1075 methyl-phenyl fluid (sale of General Electric company) and 556 cosmetics-stage fluids (sale of DowCorning company).Available polyether siloxane copolymer comprises, for example, the viscosity under 25 ℃ is the polyoxy alkylidene ether copolymer of about 1200 to 1500 centistokes.This fluid can SF1066 organosiloxane surfactant (sale of General Electric company) form obtain.Polysiloxanes glycol ether copolymer is to can be used for preferred copolymer of the present invention.

Can be used for non-volatile paraffin oils of the present invention and comprise mineral oil and some branched-chain hydrocarbons.This fluidic example is disclosed in US patent 5,019,375 (Tanner etc., 1991.5.28 authorizes), and its integral body is incorporated herein by reference.Preferred mineral oils has following feature:

Viscosity under (1) 40 ℃ is that about 5 centistokes are to about 70 centistokes;

Density under (2) 25 ℃ is about 0.82 to 0.89g/cm ³

(3) flash-point is about 138 ℃ to about 216 ℃; And

(4) carbon chain lengths is about 14 to about 40 carbon atoms.

Preferred side chain hydrocarbon ils has following feature:

Density under (1) 20 ℃ is about 0.79 to about 0.89g/cm ³

(2) boiling point is greater than about 250 ℃; And

(3) flash-point is about 110 ℃ to about 200 ℃.

Particularly preferred branched-chain hydrocarbons comprises Permethyl 103 A, and it contains average about 24 carbon atoms; Permethyl 104A, it contains average about 68 carbon atoms; Permethyl 102A, it contains average about 20 carbon atoms; All all buy the company from Permethyl; And Ethylflo 364, it contains the mixture of 30 carbon atoms and 40 carbon atoms and can buy the company from Ethyl.

Other can be used for solvent of the present invention and sees US patent 5,750,096 (Gerald J.Guskey etc., 1998.5.12 authorizes), and its integral body is incorporated herein by reference.

Water

Preferably, cosmetic composition water content of the present invention is from about 1% to about 95%, preferably from about 5% to about 90%, and more preferably from about 10% to about 85%.

Optional components

Gloss controlling agent

The cosmetics of improvement and/or adjusting skin glossy appearance situation more and more are subjected to the welcome of consumer, are meant " gloss controlling agent " referred in this.Can comprise gloss controlling agent in the compositions of the present invention.

Frequent tedious state is " oily skin ", and this is because excess sebum and hidropoiesis cause to the skin.Sebum is kind of an oil mixture, comprises Squalene, triglyceride, fatty acid and wax ester basically.Sebum is produced by the sebaceous gland of skin.Oily skin and gloss, tedious outward appearance and disgusting touch feeling link together.Antiperspirant mainly is water, wherein contains the inorganic salt for example sodium chloride and the potassium chloride of the solubility of trace.

Typically, gloss controlling agent is porous in essence.After they are coated on the skin, just provide and store up layer, thereby reduce the visible water yield on the skin in the excessive moisture absorption hand-hole.

Without being limited by theory, it is generally acknowledged that effective porous absorbent material and being used in combination of no absorbability ball-type material are preferred.The latter emphasizes the scattered reflection effect on the problematic direct reflection, causes the glossy appearance that therefore optical change of skin is also reduced skin.Being used in combination of absorbent and no absorbability spherical particles is preferred, and this is because it provides the optimum gloss control of product development, also provides product to have best tactile property.

Suitable gloss controlling agent comprises but does not limit to silicon dioxide, zeopan, Talcum, sericite and multiple organic copolymer.Especially effectively gloss controlling agent comprises silicate or carbonate, and they are by carbonate or silicate and alkali metal, alkaline-earth metal or transition metal and Silicon stone (silicon dioxide) reaction and form.Preferred gloss controlling agent is chosen from the set that comprises calcium silicates, amorphous silica, calcium carbonate, magnesium carbonate, zinc carbonate and compositions thereof.The silicate that the present invention adopts or some particular example of carbonate the 4th edition, have in the 155th, 169,556 and 849 pages (1984) more fully and explain at the chemistry encyclopedia of Van NostrandReinhold.

The gloss controlling agent of synthesis type is preferred, especially silicate.Suitable carbonate synthesis salt is commercially available in Mallinckrodt or Whittaker, Clarke﹠amp; Daniels.The example of the synthesis type silicate that the present invention uses is Hubersorb 250  or Hubersorb 600 , is available commercially from JM Huber.

When being used for moisture and gloss control, the gloss controlling agent that mainly comprises silicon dioxide will be preferable over the material that those mainly comprise silicate and/or carbonate.Most preferred silicon dioxide are the forms with microsphere and/or spheroid, have found that they have also to help except effective moisture absorption to the good tactile characteristic of skin.The silicon dioxide spheroid that the present invention uses can be available commercially from DuPont such as ZELEC Sil, also can be available commercially from Kobo such as SilicaShells.The silicon dioxide microsphere body is commercially available in Kobo such as MSS-500, MSS500/3, MSS-500H, MSS500/3N, MSS-500N and MSS 500/3N; PresperseSpheron L1500, Spheron P1500.Fumed silica also can use together with the Cab-O-Sil of Aerosil that is available commercially from Degussa and Cabot, and the both is particularly useful.

In silicate series, zeopan is useful, and particularly Sebumase is commercially available in Miyoshi Kasei.

When silicon dioxide when particularly silicon dioxide spheroid and silicon dioxide microsphere body are as the main means of moisture absorption, preferably, weight based on compositions, absorb the content from about 1% to about 40% of silicon dioxide in the powder, more preferably from about 1% to about 25%, most preferably approximately from 2% to about 10%.

Starch-based materials also can be used as gloss controlling agent.Useful examples is Natrosorb W and Natrosorb HFW, and DryFlo plus and DryFlo AF pure are commercially available in national starch and chemical company.

The polymeric material of also finding methacrylate based plinth is useful.They can be used for being used in combination with the dimethyl polysiloxane copolymer, or as the copolymer of methacrylate based plinth.Especially, useful examples is: Microsponge 5640w.Glycerin, and Polytrap6603, commercially available in Enhanced Derm technologies; DSPCS-I2 series and SPCAT-I2, commercially available in Kobo; Poly-Pore200 series, commercially available in Amcol.

Alternatively, also be preferably, compositions of the present invention comprises spheroidal particle, and its mean diameter is 10 microns or bigger, and is preferably greater than 15 microns, preferred greater than 20 microns.Particle diameter can be regarded as basic or primary granule.

Preferred spheroidal particle is including, but not limited to the aggregated particles of choosing from methyl silsesquioxane resin microsphere body, and for example Toshiba silicone sells 0 microsphere with trade name Tospearl 145A; Poly (methyl methacrylate) micro-sphere, for example Seppic is with the microsphere of trade name MicropearlM 100 sales; Crosslinked poly dimethyl polysiloxanes spheroidal particle, the particularly spheroidal particle of selling with trade name Trefil E 506C or Trefil E 505C as DowCorning Toray Silicone; Polyamide spheroidal particle and nylon 12 more particularly, the particularly spheroidal particle of selling with trade name Orgasol 2002D Nat C05 as Atochem; The polystyrene microsphere body, for example Dyno Particles is with the microsphere of trade name Dynospheres sale; Ethylene acrylate copolymer that Kobo sells with trade name FloBead EA209 and composition thereof.The Ronasphere that also finds Kobo company is useful.

Preferably, the concentration of spheroidal particle from about 0% to about 40%, preferred from about 5% to about 35%, most preferred from about 8% to about 30%.

Film former

Film former is the selectable components that the present composition comprises, and it helps the affinity of thin film and skin and is attached on the skin.Improve the permanent durable and non-transmission performance of this compositions expects very much.Water miscible, water-insoluble and water dispersible film former all can use and provide satisfactory final benefit in the inner phase of this compositions and foreign minister.

Preferably, based on the weight of compositions, be contained in the content from about 0% to about 20%, preferred from about 0.1% to about 10%, most preferred from about 0.1% to about 5% of the film former of compositions.

Suitable film former comprises:

1) organic siliconresin, the silicon fluoride resin, the organic siliconresin copolymer, for example, be available commercially from the trimethyl silyloxy silicate (SR1000) of GE, the organic siliconresin copolymer of GE, for example, SF1318 (silicones and isostearic acid organic ester copolymer) and CF1301 (silicones and αJia Jibenyixi copolymer), the copolymer of the contact adhesive-silicones of Dow Corning and different PDMS (BIO-PSA series); With

2) acrylic acid and metha crylic polymer and resin, silicon-acrylate type copolymer and fluoridize type comprises the siloxanes addition polymerization compound SA70 that is available commercially from 3M, be available commercially from the KP545 of Shin-Etsu, alkyl acrylate copolymer for example, is available commercially from the KP561 and 562 of Shin-Etsu.

3) be available commercially from decene/butylene copolymer of Collaborative Labs.

4) material on polyvinyl compound basis, for example, PVP, PVP/VA comprises the Antaron/Ganex (PVP/Triacontene copolymer) that is available commercially from ISP, is available commercially from the Luviskol material of BASF.

5) polyurethane for example, is available commercially from the Polyderm series of Alzo, includes but not limited to Polyderm PE/PA, Polyderm PPI-SI-WS, PolydermPPI-GH, is available commercially from the Luviset P.U.R. of BASF;

6) polyquaternary amine material for example is available commercially from the Luvisquat series of BASF.

7) acrylate copolymer and acrylate/acrylamide copolymer, for example Luvimer and Ultrahold series are all commercially available in BASF;

8) material on styrene basis; With

9) material of chitosan and chitosan based comprises the material on cellulose and cellulose basis.

For example exist International cosmetic ingredient dictionary and handbook, the 7th edition, volume 2 discloses this type of film former in the 1636-1638 page or leaf.

Skin conditioning agent

Alternatively, compositions of the present invention further comprises skin conditioning agent.These medicaments can be chosen from wetting agent, horny layer remover or emollient.

Wetting agent is a polyhydroxy-alcohol, and in order to moisturize, minimizing is peeled off with chafe and increased removing of scale.Typical polyhydroxy-alcohol comprises polyalkylene glycol, more preferably alkylidene polyol and derivant thereof.Illustrative is propylene glycol, dipropylene glycol, polypropylene glycol, Polyethylene Glycol, sorbitol, hydroxypropyl sorbitol, hexanediol, 1,3 butylene glycol, 1,2,6-hexanetriol, ethoxylated glycerol, propoxylated glycerol and composition thereof.Most preferred wetting agent is a glycerol.When existing, the weight content scope from 1% to 50% of wetting agent, preferably from 10% to 40%, best from 25% to 35%.

Remover of the present invention can be selected from the C2-C30 alpha-hydroxy carboxylic acid compounds, beta-hydroxycarboxylic acids and these sour salt.First-selected is glycolic, lactic acid and salicylic acid and their ammonium salt.The amount of keratodermatitis remover can be 1 to 15wt%, and preferred 2 to 10wt%.

Can use various C2-C30 alpha-hydroxy carboxylic acid compounds.Its suitable example comprises:

Alpha-hydroxy acetic acid

α-Qiang Jibingsuan

The Alpha-hydroxy caproic acid

Alpha-hydroxy is sad

The Alpha-hydroxy capric acid

The Alpha-hydroxy dodecylic acid

The Alpha-hydroxy tetradecanoic acid

The Alpha-hydroxy hexadecanoic acid

The Alpha-hydroxy octadecanoid acid

The Alpha-hydroxy arachic acid

The Alpha-hydroxy behenic acid

The Alpha-hydroxy hexacosoic acid and

The Alpha-hydroxy octocosoic acid

When conditioner was emollient, it can be selected from hydrocarbon, fatty acid, aliphatic alcohol and ester.Isononyl isononanoate is first-selected hydrocarbon type emollient conditioner.Operable other hydrocarbon comprises mineral oil, polyolefin such as poly decene and alkane such as 2-Methylpentadecane (for example Permethyl 99 registered trade marks and Permethyl 101 registered trade marks).Preferably, compositions of the present invention is substantially free of semi-solid hydrocarbon, as vaseline, lanoline and lanolin derivative, and sterol (for example, the ethoxylation soyasterol), high molecular polybutene and Oleum Cocois.Among the present invention, " being substantially free of " means the concentration of semisolid hydrocarbon preferably less than 10%, is more preferably less than 5%, and be first-selected less than 2% and to be more preferably be 0.Need not theoretical to support that this semi-solid hydrocarbon tends to cover the sense organ benefit of silicone elastomer composition, as non-greasy of the present invention, relaxed and comfortable sensation.

Fatty acid and aliphatic alcohol have 10 to 30 carbon atoms.The illustrative examples of this class material is n-nonanoic acid, lauric acid, myristic acid, Palmic acid, stearic acid, isostearic acid, hydroxy stearic acid, oleic acid, linoleic acid, castor oil acid, arachidic acid, behenic acid and erucic acid and corresponding alcohol.

Oily ester type emollient can be selected from one or more of following ester:

1, triglyceride is as plant and animal fat and oily.Example comprises Oleum Ricini, safflower oil, Oleum Gossypii semen, Semen Maydis oil, olive oil, cod-liver oil, almond oil, American Avocado Tree oil, Petiolus Trachycarpi oil, Oleum sesami, Squalene, Kikui oil and soybean oil.

2. aceto-glyceride is as acetylizad glyceryl monoacetate.

3. ethoxylated glycerol ester is as the ethoxylation glyceryl monostearate.

4.10 Arrcostab to 20 carbon atom fatty acids.The methyl of fatty acid, isopropyl and butyl ester all can be used for the present invention.Example comprises lauric acid hexyl ester, lauric acid dissident ester, Palmic acid dissident ester, isopropyl palmitate, decyl oleate, Ceraphyl 140A, the stearic acid cetyl ester, stearic acid ester in the last of the ten Heavenly stems, isostearic acid isopropyl ester, diisopropyl adipate, adipic acid two dissident's esters, adipic acid dihexyl ester in the last of the ten Heavenly stems, Dermol DIPS, Lauryl lactate, Tetradecyl lactate and lactic acid cetyl.

5.10 alkenyl ester to 20 carbon atom fatty acids.The example comprises the myristic acid grease, stearic acid grease and Cetiol.

6. ether-ester is as the fatty acid ester of ethoxylized fatty alcohol.

7. polyol ester.Ethylene glycol one and two-fatty acid ester, diethylene glycol one-and two-fatty acid ester, Polyethylene Glycol (200-6000) one-and two-fatty acid ester, propylene glycol one-and two-fatty acid ester, polypropylene glycol 2000 monooleates, polypropylene glycol 2000 monostearates, ethoxylation propylene glycol monostearate, glycerol one-and two-fatty acid ester, polyglycereol fattiness acid (polyfatty) ester, the ethoxylation glyceryl monostearate, 1,2-butanediol monostearate, 1,2-butanediol distearate, the polyethylene glycol oxide polyol fatty acid ester, fatty acid esters of sorbitan and polyethylene glycol oxide fatty acid esters of sorbitan are gratifying polyol esters.

8. wax ester, as Cera Flava, spermaceti, myristyl myristate, the stearic acid stearyl.

9. the sugar and the C of related substances ₁-C ₃₀One ester or polyester.These esters are made of sugar or polyol moiety and one or more carboxylic moiety.Depend on that structure divides acid and sugared, these esters at room temperature can be the liquid or solid forms.The example of liquid ester comprises: glucose four oleates, the glucose tetra-ester of soya fatty acid (unsaturated), mannose four esters of mixing soya beans fatty acid oil, oleic galactose four esters, linoleic arabinose four esters, xylose four linoleates, galactose five oleates, sorbitol four oleates, sorbitol six esters of unsaturated soya fatty acid, xylitol five oleates, sucrose four oleates, sucrose five oleates, sucrose six oleates, sucrose seven oleates, sucrose eight oleates and composition thereof.The example of solid ester comprises: sorbitol six esters, and wherein carboxylate moiety is the palm acid ester and the Arachidate of 1: 2 mol ratio; The octaester of Raffinose, wherein carboxylate moiety is the linoleate and the docosane acid esters of 1: 3 mol ratio; Seven esters of maltose, the carboxylic moiety that wherein is used for esterification are the Semen Helianthi fatty acid oil and the lignocerane acid groups of 3: 4 mol ratios; The octaester of sucrose, the carboxylic moiety that wherein is used for esterification are the oleic acid root and the docosane acid groups of 1: 3 mol ratio; And the octaester of sucrose, the carboxylic moiety that wherein is used for esterification is laurate, linoleate and the docosane acid group of 1: 3: 4 mol ratio.Preferred solid material is a sucrose polyfatty acid esters, and wherein degree of esterification is 7-8, and fatty acid part wherein is C18 one-and/or two-unsaturated acids and behenic acid, and unsaturated acids: the mol ratio of behenic acid is 1: 7 to 3: 5.The octaester that a kind of particularly preferred sugar cube polyester is a sucrose, the fatty acid part of 7 behenic acids of wherein having an appointment in the molecule and about 1 oleic acid part.Other material comprises the Oleum Gossypii semen or the soya fatty acid ester of sucrose.This ester type material also is described in US patent 2,831,854, US patent 4,005,196 (Jandacek, 1977.1.25 authorizes); US patent 4,005,195 (Jandacek, 1977.1.25 authorizes), US patent 5,306,516 (Letton etc., 1994.4.26 authorizes); US patent 5,306,515 (Letton etc., 1994.4.26 authorizes); US patent 5,305,514 (Letton etc., 1994.4.26 authorizes); US patent 4,797,300 (Jandacek etc., 1989.1.10 authorizes); US patent 3,963,699 (Rizzi etc., 1976.6.15 authorizes); US patent 4,518,772 (Volpenhein, 1985.5.21 authorizes) and US patent 4,517,360 (Volpenhein, 1985.5.21 authorizes).

The amount of skin conditioning agent can be about 0wt% to 30wt%, and preferably about 1wt% is about 20wt% extremely, best about 1wt% to 10wt%.

Firming agent

Can contain one or more in the cosmetic composition of the present invention and can effectively make particular fluid base material solidified material used in the cosmetic composition, separately or be referred to as " firming agent " at this.(among the present invention, term " curing " instigates liquid base material to form solid-state or semi-solid physics and/or chemical transformation under environmental condition, that is, form and to have stable physical arrangement and at the final composition of regular service conditions deposit on skin.) those skilled in the art will know that, for the particular type (that is being base material with gel or wax) of desired composition, required rheological characteristic, used liquid base material and other material of desiring to use are depended in the selection of the specific firming agent that uses in cosmetic composition in compositions.Firming agent preferably with about 0 to about 90%, more preferably from about 1 to about 50%, be more preferably about 5% and exist to about concentration of 40%, first-selected about 1% to about 15%.

Suitable firming agent comprises the waxiness material, as candelilla wax, and Brazil wax, Cera Flava, spermaceti, babassu, Fructus Lauri nobilis wax (baysberry), montan wax, ceresine, ceresin, paraffin, synthetic wax such as Fisher-Tropsch wax, siloxane wax is (for example, the DC 2503 of Dow Corning), microwax or the like; The soap class is as the sodium salt and the potassium salt of higher fatty acids (acid that promptly has the 12-22 carbon atom); The amide of higher fatty acids; The higher fatty acid amides of alkanolamine; Two benzaldehydes-one sorbitol acetal; The acetate of alkali metal and alkaline-earth metal, propionate and lactate; And their mixture.Also can use polymer material, as locust bean gum, sodium alginate, sodium caseinate, the albumin of egg, gelatin agar, the carrageenin sodium alginate, xanthan gum ， Quince smoke tree seed extract, Tragacanth, starch, starch of chemical modification or the like, semisynthetic polymer material is as cellulose ether (for example, hydroxyethyl-cellulose, methylcellulose, hydroxypropyl cellulose, carboxymethyl cellulose, hydroxypropyl emthylcellulose), polyvinyl pyrrolidone, polyvinyl alcohol, guar gum, hydroxypropyl guar locust beam gum, soluble starch, cationic cellulose, cation guar gum or the like and synthetic polymer material are as CVP Carbopol ETD2050, polyvinyl pyrrolidone, the polyvinyl alcohol acrylic acid polymer, polymethacrylic acid polymer, polyvinyl acetate ester polymer, polyvinyl chloride polymer, polyvinylidene chloride polymer or the like.Inorganic thickening agent also can use, as the aluminosilicate-type chemical compound, for example, the mixture of bentonite or Polyethylene Glycol and polyglycol distearate or distearate.Naturally occurring polymer or biopolymer and uses thereof further describe in EP application 522624 (Dunphy etc.).The visible Cosmetic Bench of other example Reference of naturally occurring polymer or biopolymer, pp.1.40-1.42 is incorporated herein by reference.

Available hydrophilic gelling agent in addition is acrylic acid/ethyl acrylate copolymer and the CVP Carbopol ETD2050 that trade name is sold as B.F.Goodrich company with Carbopol registered trade mark resin.These resins are formed wherein said cross-linking agent such as polyene propyl group sucrose or polyene propyl group tetramethylolmethane by the crosslinked colloidal state water-soluble poly alkenyl polyether cross linked polymer of acrylic acid and 0.75% to 2.00% cross-linking agent basically.Example comprises Carbopol 934, Carbopol940, and Carbopol 950, and Carbopol 980, Carbopol 951 and Carbopol 981.Carbopol 934 is acrylic acid and the mutually crosslinked water-soluble polymer of the polyallyl ether of about 1% sucrose, and every sucrose molecule has average about 5.8 pi-allyls in the wherein said sucrose.Be applicable to (the CTFA name: the Carbomers of Chu Shouing acrylate/10-30 alkyl acrylate cross-linked polymer) that also has of the present invention with trade name Carbopol Ultrez 10, Carbopol ETD2020, Carbopol 1382, Carbopol 1342 and Pemulen TR-1.Above-mentioned polymer also can be united use in the present invention.The gellant that other suitable the present invention uses comprises oleogel such as trihydroxy tristerin.

The hydrophobically modified cellulose also is suitable for the present invention.These celluloses are in US patent 4,228,277 and 5,104, have a detailed description in 646, and these two pieces of whole integral body are incorporated herein by reference.

P.1.27 the suitable gellant or the visible Cosmetic BenchReference of other example of gelatinizing agent, are incorporated herein by reference.

Other example of suitable firming agent be disclosed in below with reference in, all are incorporated herein by reference: US patent 4,151,272 (Geary etc., 1979.4.24 authorizes); US patent 4,229,432 (Geria, 1980.10.21 authorizes) and US patent 4,280,994 (Turney, 1981.7.28 authorizes); " chemistry of wax and technology (The Chemistry and Technology ofWaxes) ", A.H.Warth, the 2nd edition, 1960 reprint, Reinhold publishing company, pp391-393 and 421; " petro chemical industry (The Petroleum Chemicals Industry) ", R.F.Goldstein and A.L.Waddeam, the 3rd edition (1967), E ﹠amp; F.N.Span Ltd., pp 33-40; " chemistry of cosmetics and manufacturing (The Chemistry and Manufacture ofCosmetic) ", M.G.DeNavarre, the 2nd edition (1970), Van Nostrand ﹠amp; Company, pp 354-376 and " encyclopedia of chemical technology (Encylopedia ofChemical Technology) " Vol.24, Kirk-Othmer, the 3rd edition (1979) pp466-481; US patent 4,126,679 (Davy etc., 1978.11.21 authorizes); EP patent application 117,070 (May, 1984.8.29 is open); US patent 2,900,306 (Slater, 1959.8.18 authorizes); US patent 3,255,082 (Barton, 1966.6.7 authorizes); US patent 4,137,306 (Rubino etc., 1979.1.30 authorizes); US patent 4,154,816 (Roehl etc., 1979.5.15 authorizes); US patent 4,226,889 (Yuhas, 1980.10.7 authorizes); US patent 4,346,079 (Roehl, 1982.8.24 authorizes); US patent 4,383,988 (Teng etc., 1983.5.17 authorizes); EP patent application 107,330 (Luebbe etc., 1984.5.2 is open); EP patent application 24,365 (Sampson, etc., 1981.3.4 is open) and US patent application serial number 630,790 (DiPietro, 1984.7.13 application)

Preferably, the hardness number of the present composition is measured with TA-XT2i texture analysis instrument (describing below) and mostly is about 25 fors most, and more preferably from about 0.5 to about 20 fors, and first-selected about 1 to about 15, and best about 1 to about 10 fors.Need not theoretical the support, it is believed that the compositions that has greater than 25 fors rods hardness (stick hardness) value tends to hinder formation by membrane structure that silicone elastomer provided, thus, can prevent slickness and intramembranous particles Uniformity of Distribution and uniformity.Thereby, the sense organ beneficial effect of adverse effect cross linking polysiloxane elastomeric component.

Coloring agent

Contain in certain embodiments of the present invention and have an appointment 0% to about 30%, preferred about 1% to about 20%, more preferably from about 2% to about 15% and first-selected about 5% to about 15% coloring agent, in anhydrous pigment weight.They are aluminum, barium or calcium salt or color lake normally.Preferably, there are about 0% to about 3% dyestuff and 0% to about 10% pearling agent.

Can be used for coloring agent of the present invention is all inorganic and organic toner/pigment that are adapted at using in the cosmetic composition.When adopting pigment, for its good dispersion, pigment generally is dispersed in the emollient in the time of in introducing lip compositions of the present invention, so that the uniform distribution of colorant to be provided.The color lake is the pigment of expanding or lightening with solid diluent, or is deposited in the organic pigment for preparing on the adsorptivity surface by water-soluble dye, and it is aluminium hydroxide normally.In some cases, soluble dye whether can be deposited in form on the surface of aluminium hydroxide the dyeing inorganic pigment or not only in the presence of substrate precipitation be uncertain.The precipitation of the insoluble salt that the color lake also can be formed by acidity or basic stain forms.Also can use calcium and barium color lake.

Be suitable for color lake of the present invention and comprise red 3 aluminum color lakes, red 21 aluminum color lakes, red 27 aluminum color lakes, red 28 aluminum color lakes, red 33 aluminum color lakes, yellow 5 aluminum color lakes, yellow 6 aluminum color lakes, yellow 10 aluminum color lakes, orange 5 aluminum color lakes and blue 1 aluminum color lake, red 6 barium color lakes, red 7 calcium color lakes.

Also can comprise other colorant in the lip pomade of the present invention, as dyestuff.Suitable example comprises redness 6, and redness 21 is brown, bronzing and yellowish-brown dyestuff and composition thereof.

Have no particular limits for the pigment in this compositions, colorant or casting resin powder.Every kind of all body pigment, inorganic Chinese white, inorganic color pigment, pearling agent and similar material.Special example is Talcum, Muscovitum, magnesium carbonate, calcium carbonate, magnesium silicate, aluminium-magnesium silicate, silicon dioxide, titanium dioxide, zinc oxide, iron oxide red, iron oxide yellow, iron oxide black, ultramarine, polyethylene powder, methacrylate powder, polystyrene powder, silk powder, crystalline cellulose, starch, metatitanic acid Muscovitum, ferrum oxide metatitanic acid Muscovitum, Bismuth Oxychloride and similar material.

Additional pigment filler includes but not limited to that organic powder is such as natural gum, Chalk, fuller earth, Kaolin, sericite, white mica, phlogopite, synthetic mica, lepidolite, biotite, lepidolite, Vermiculitum, aluminium silicate, starch, smectic clays, alkyl and/or trialkyl aryl terre verte, the aluminium-magnesium silicate of chemical modification, organically-modified montorillonite clay, aluminium hydrosilicate, calcine aluminum starch ocentyl succinic barium silicate, calcium silicates, magnesium silicate, strontium silicate, metal tungstates, magnesium, silica alumina, zeolite, barium sulfate, calcined calcium sulfate hemihydrate (calcined gypsum), calcium phosphate, fluoridated apatite, hydroxyapatite, the pottery powder, metallic soap (zinc stearate, magnesium stearate, Grillocin P 176, calcium palmitate and aluminium stearate), silica sol, and boron nitride; Organic powder such as polyamide powder (nylon powder), cyclodextrin, methyl polymethacrylates powder, styrene and acrylic acid copolymer medicinal powder, benzoguanamine resin powder, poly-(ethylene tetrafluoride) powder and carboxy vinyl polymer, cellulose powder such as hydroxyethyl-cellulose and Carboxymethyl cellulose sodium, ethylene glycol monostearate; Inorganic Chinese white is such as magnesium oxide, but is not limited to these.Authorize people's such as El-Nokaly United States Patent (USP) 5,688,831 to introduce other useful powder on November 18th, 1997, completely be introduced in Insert Here by it.These pigment and powder can independently use or unite use.

Also can be used for herein pigment and/or dyestuff capsule arranged, as nano-coloring material (nanocolorants) and the multi-coated interference pigment of BASF, as Sicopearls from BASF.

Preferably pigment is carried out surface treatment, and then extra colour stability is provided and is convenient to preparation.The pigment of hydrophobic treatment is preferred, because of it can more easily disperse in solvent/oil phase.In addition, it may be useful by the material mutually compatible with polysiloxanes pigment being handled.Especially, the hydrophobic pigment that is particularly useful that uses in polysiloxanes bag aqueous emulsion is handled and is comprised as United States Patent (USP) 5,143, and the polysiloxanes of introducing in 722 is handled, and completely is introduced in Insert Here by it.The primary average particle size of same preferred pigment from about 10nm to about 100,000nm, more preferably from about 50nm to about 5000nm, most preferably from about 100nm to about 1000nm.The identical or different mixture with pigment with different-grain diameter also is useful (for example adding TiO2 and primary particle diameter the TiO2 from about 10nm to about 50nm of primary particle diameter from about 100nm to about 400nm) at this.

Dispersant also can with colorant among the present invention and pigment is collaborative uses, and suitable dispersant is including, but not limited at United States Patent (USP) 5,688, and the dispersant of statement in 493 completely is introduced in Insert Here by it.

Antiseptic

The traditional preservatives that is fit to compositions of the present invention is the Arrcostab of P-hydroxybenzoic acid.Other antiseptic of more uses recently comprises hydantoin derivatives as 1,3-two (hydroxymethyl)-5,5-dimethyl hydantoin, propionate and various quaternary ammonium compound, as alkyl benzyl dimethyl ammonium chloride, Quaternium 15 (Dowicil 200), benzethonium chloride and methyl benzethonium chloride.The cosmetic chemistry man is familiar with suitable antiseptic and routine selects them to satisfy the stability that product was tested and provided to the antiseptic problem.Particularly preferred antiseptic is the EDTA disodium, phenyl phenol, methyl parahydroxybenzoate, propyl p-hydroxybenzoate, imidazolidinyl urea (can Germall 1157 commercially available), dehydro sodium acetate and benzyl alcohol.Should consider in the purposes of compositions and antiseptic and the emulsion possible incompatibility between other composition when selecting antiseptic.The use amount of antiseptic be preferably composition weight about 0% to about 5%, more preferably from about 0.01% to about 2.5%, first-selected about 0.01% to about 1%.

Emulsifying agent

Except the emulsification and cross linked silicone elastomer, the present invention can also use other emulsifying agent or surfactant.These emulsifying agents can be nonionic, anion or cationic.Examples of suitable emulsifiers is disclosed in, for example, and US patent 3,755,560 (1973.8.28 authorizes, Dickert etc.); US patent 4,421,769 (1983.12.20 authorizes, Dixon etc.) and McCutcheon ' sDetergents and Emulsifiers, the North America version, 317-324 page or leaf (1986), integral body is incorporated herein by reference separately.Exemplary non-ionic surface active agent is to be the oxyalkylated chemical compound and the anhydro sorbitol of base material with C10-C22 aliphatic alcohol and acid.These materials can obtain certainly, and for example Shell Chemical company is a trade mark with Neodol.The present invention can use also sometimes that BASF AG sells with the polypropylene oxide-polyoxyethylene alkene copolymer of Pluronic as trade mark.Can obtain also can be used in the present invention from the alkyl polyglucoside of Henkel company.Anionic emulsifier or surfactant comprise fatty acid soaps, sodium lauryl sulfate, and sodium laureth sulfate, alkylbenzenesulfonate, one-and two-alkyl acid phosphate and Igepon A.Amphoteric emulsifier or surfactant comprise such as dialkyl group amine oxide and various types of betanin (as cocamidopropyl betaine).

Being preferred for of the present invention is the poly (oxyalkylene) base co-polymer, also is known as polyether silicon.Polymer has a detailed description in US patent 4,268,499, and its integral body is incorporated herein by reference.Particularly preferred poly (oxyalkylene) base co-polymer is known with its CTFA called after dimethicone copolyol.A particularly preferred form of dimethicone copolyol is provided with DC5225C by Dow Corning.

The total concentration of emulsifying agent can be preparation 0% to about 10%, 0.1% to about 5% and first-selected about 0.1% to about 2% of preferred composition weight.The visible US patent 5,085,856 of the example of examples of suitable emulsifiers (Dunphy etc.); The clear 61-83110 of JP patent publication No.; EP patent application EP 522624 (Dunphy etc.); US patent 5,688,831 (El-Nokaly etc.); And the visible Cosmetic Bench of the example Reference of suitable humidizer (moistures), pp.1.22,1.24-1.26 (1996), all these equal integral body are incorporated herein by reference.

The organic sunscreen agent

The present composition preferably comprises organic sunscreen.Suitable sunscreen can have UVA absorbent properties, UVB absorbent properties or its combination.The definite consumption of sunscreen actives is decided with desired sun protection factor (being " SPF " of compositions) and desired UVA protection level.The present composition preferably comprises at least 10, preferred at least 15 SPF.(SPF normally is used for weighing the photoprotection functioning efficiency that sunscreen prevents to occur because of solar radiation erythema, and SPF is defined as: the ratio that occurs identical minimum erythema required ultraviolet light energy on the skin that scribbles sunscreen on the same individuality and the skin that is not coated with sunscreen.See Federal Register, 43, No.166, pp.38206-38269, on August 25th, 1978).Preferably, calculate by weight, the organic sunscreen agent content is from about 2% to about 20% in the present composition, and more typical is from about 4% to about 14%.Suitable sunscreen comprise those can The international cosmetic composition of CTFA Dictionary and handbook, the 7th edition, roll up 2,1672 pages, the author finds among Wenninger and the McEwen (cosmetics, toilet articles and fragrance association company, Washington D.C., 1997), but is not limited thereto.

Preferably, comprise UVA in the compositions of the present invention and absorb the sunscreen actives agent, it can the ultraviolet radiation of absorbing wavelength scope from about 320nm to about 400nm.It is from the dibenzoyl methane derivant that suitable UVA absorbs the sunscreen actives agent, and the o-aminobenzoa derivant is methyl o-aminobenzoa and high methyl for example, 1-N-acetyl group o-aminobenzoa and composition thereof.The example of dibenzoyl methane sunscreen actives agent has description in the United States Patent (USP) 4,387,089 of authorizing Depolo; With in " sunscreen: development, assessment and management aspect " (N.J.Lowe and N.A.Shaath work, Marcel Dekker company, 1990) book, description is arranged.Preferably existing a certain amount of UVA to absorb the sunscreen actives agent provides protection to wide range UVA, this activating agent or independent the use, perhaps with this compositions in other ultra-violet protecting agents that may exist unite use.

The agent of preferred UVA sunscreen actives is agent of dibenzoyl methane sunscreen actives and derivant thereof.Include but are not limited to: 2-methyldiphenyl formyl methane, 4-methyldiphenyl formyl methane, 4-isopropyl diphenyl formyl methane, 4-tert-butyl group dibenzoyl methane, 2,4-dimethyl dibenzoyl methane, 2,5-dimethyl dibenzoyl methane, 4,4 '-the diisopropyl dibenzoyl methane, (4-(1, the 1-dimethyl ethyl)-4 '-methoxy dibenzoyl methane, 2-methyl-5-isopropyl-4 '-methoxy dibenzoyl methane, 2-methyl-5-the tert-butyl group-4 '-methoxy dibenzoyl methane, 2,4-dimethyl-4 '-methoxy dibenzoyl methane, 2,6-dimethyl-4 '-tert-butyl group-4 '-sunscreen actives of methoxy dibenzoyl methane and their mixture.Preferred dibenzoyl sunscreen actives comprises and is selected from following chemical compound: 4-(1, the 1-dimethyl ethyl)-4 '-methoxy dibenzoyl methane, isopropyl diphenyl formyl methane and their mixture.4-(1, the 1-dimethyl ethyl)-4 '-methoxy dibenzoyl methane is preferred.

Sunscreen actives 4-(1, the 1-dimethyl ethyl)-4 '-methoxy dibenzoyl methane also is usually said Uvinul BMBM or Avobenzone, can trade name Parsol ^1789 from Givaudan-Roure (International) S.A. (Basel, SUI) with trade name Eusolex ^9020 from Merck ﹠amp; Co.Inc. (Whitehouse Station NJ.) buys.Sunscreen actives 4-isopropyl diphenyl formyl methane also is usually said isopropyl diphenyl formyl methane, can trade name Eusolex ^8020 buy from Merck.

Preferably, comprise the agent of UVB sunscreen actives in the compositions of the present invention, it can the ultraviolet radiation of absorbing wavelength from about 290nm to about 320nm.Preferably, compositions comprises the agent of a certain amount of UVB sunscreen actives, perhaps independent the use, perhaps with this compositions in other ultra-violet protecting agents that may exist unite use, UVB can be provided protection safely and effectively.Preferably, calculate by weight, the content of the UVB absorbability organic sunscreen agent that comprises in the compositions is from about 0.1% to about 16%, and is preferred from about 0.1% to about 12%, and most preferably from about 0.5% to about 8%.

In this many kinds of UVB sunscreen actives agent is suitable the use.The limiting examples of this type of organic sunscreen actives authorizes people's such as Haffey United States Patent (USP) 5,087,372 and December in 1991 to authorize in 17th in people's such as Turner the United States Patent (USP) 5,073,371,5,073,372 on February 11st, 1992 have description.The agent of preferred UVB sunscreen actives is from 2-ethylhexyl-2-cyano group-3,3-diphenylacrylate ester (being called octocrilene), 2-phenyl-benzimidazole-5-sulfonic acid (PBSA), cinnamate and derivant thereof be 2-ethylhexyl-p-Methoxycinnamate and octyl group-p-Methoxycinnamate for example, the TEA salicylate, octyldimethyl PABA, camphor derivatives and their derivant, and above-mentioned mixture is select.Preferred organic sunscreen actives is 2-ethylhexyl-2-cyano group-3,3-diphenylacrylate ester (being called octocrilene), 2-phenyl-benzimidazole-5-sulfonic acid (PBSA), octyl group-p-Methoxycinnamate and composition thereof.Acid sunscreen with form in salt and the acid also is useful at this.When using organic sunscreen agent salt such as PBSA in synthetic of the present invention, they can disturb the effect of thickening agent, and the result is that final products have the suboptimum rheology.This phenomenon can be offseted by increasing more high-load thickening agent, aliphatic alcohol or non-ionic surfactant, and the rheology of final products can be recovered desired horizontal like this.

Also can add reagent in the present invention in useful any compositions, in order to stablizing the UVA sunscreen, thereby prevent that the UVA sunscreen is exposed to the light degradation that causes under the ultraviolet radiation and keeps its UVA protection effect.A large amount of chemical compounds has been cited because of the stability characteristic (quality) that they are provided and should selected as a whole additional UVA sunscreen and the compositions done.Suitable stabilizing agent is at United States Patent (USP) 5,972,316,5,968,485,5,935,556,5,827,508 and patent WO00/06110 in state, but be not limited to this.The stabilizing agent preferred examples that the present invention uses comprises 2-ethylhexyl-2-cyano group-3,3-diphenylacrylate ester (being called octocrilene), ethyl-2-cyano group-3,3-diphenylacrylate ester, 2-ethylhexyl-3,3-diphenylacrylate ester, ethyl-3, two (4-methoxyphenyl) acrylate of 3-and composition thereof, 2-ethylhexyl-2-cyano group-3,3-diphenylacrylate ester is most preferred.

Also can add reagent in the present invention in useful any compositions, in order to improve the skin affinity of these compositionss, especially the enhancing composition opposing is washed away by water or is wiped free of.The preferred reagent that this interests can be provided is ethylene and acrylic acid copolymer.In the United States Patent (USP) 4,663,157 of mandate on May 5th, 1987 Brock, disclosed the compositions that comprises this analog copolymer.

Inorganic sunscreen

Compositions of the present invention can comprise the rational sunscreen of inorganic matter in addition except the organic sunscreen agent.The unrestricted example of proper physical sunscreen the CTFA international cosmetic ingredient dictionary (the 6th edition, 1995,1026-28 page or leaf and 1103 pages, Sayre, people such as R.M. work), " physical property sunscreen " (J.Soc.Cosmet.Chem, volume 41, No 2,103-109 page or leaf, 1990) in statement is arranged.The rational sunscreen of preferred inorganic matter is zinc oxide and titanium dioxide and composition thereof.

As when using the physical sunscreen agent, its amount should guarantee that compositions is (being non-whitening) of printing opacity, can preferably be less than or equal to 5% content approximately on skin.As what use is titanium dioxide, its available anatase, rutile or its impalpable structure.Physical sunscreen agent granule such as titanium dioxide or zinc oxide, can by or do not applied by various materials, coating substance includes but not limited to aminoacid; The chemical compound of aluminum such as aluminium oxide, aluminium stearate, Aluminum trilaurate or the like; Carboxylic acid and their salt such as stearic acid and salt thereof; Phospholipid such as lecithin; Organosilicone compounds; Inorganic silicon siloxane compound such as silicon dioxide and silicate; And their mixture.Preferred titanium dioxide can be buied from Tayca (Japan), and (Emerson NJ) distributes with MT micron particle series (as MT100SAS) by Tri-K Indursties.

Preferably, calculate by weight, in the present composition inorganic sunscreen content from about 0.1% to about 10%, more preferably from about 0.1% to about 4%, most preferably from about 0.5% to about 2.5%.

Aerated composition

Not necessarily and preferably, compositions of the present invention is inflated." inflation " means in the present invention by hands, mechanical mixture or by other form of conventional foaming or stir the bubble technical device and mix air.Preferably, contain at least about 1% in the compositions of the present invention, preferably at least about 2%, best about 3 to about 5% air.

The composition that other is nonessential

Various additional compositions can be spiked in the compositions of the present invention.The non-limiting example of these supplementary elements comprises other skin care activity thing, as peptide (for example, the Matrixyl[pentapeptide derivative]), farnesol, bisabolol, phytantriol, glycerol, urea, guanidine (for example, aminoguanidine); Vitamin and derivant thereof, as ascorbic acid, vitamin A is (for example, retinoid derivant such as retinol cetylate or retinol propionic ester), vitamin E (for example, tocopherol acetas), vitamin B3 (for example, nicotiamide) and vitamin B5 (for example, pantothenylol) or the like and composition thereof; Sunscreen; Anti-acne medicament (resorcinol, salicylic acid, or the like; Antioxidant (for example, plant sterol, thioctic acid); Flavonoid (for example, isoflavone, phytoestrogen); Skin is alleviated and consolidant, as Aloe extract, and allantoin or the like; Chelating agen and sequestering agent; And suitable aesthetic purposes use agent, as quintessence oil, aromatic, skin sensitizer (sensates), opacifier, aromatic compounds (for example, cloves oil, menthol, Camphora, Eucalyptus oil and acetaminol).The indefiniteness embodiment of suitable carboxyl copolymer, emulsifying agent, emollient and other supplementary element is disclosed in US patent 5,011,681 (Ciotti etc., 1991.4.30 authorize) and US patent 5,939,082 (Oblong etc., 1999.8.17 authorize), it all is incorporated herein by reference.The above-mentioned vitamin b 3 compound of mentioning can be with the crystal form of recrystallization so that keep crystal form or to be partly dissolved the crystal form admixture of (that is, some dissolution of crystals and some still keep crystal form in compositions) in compositions.

Analyze experimental technique

The mensuration of particle diameter

The preparation of sample is to place the cross-linked elastomer (gel) of about 1 gram and the isopropyl alcohol that about 30 gram ratios are 1: 1 in bottle: dimethyl polysiloxane (DC245) solution (IPA: DC245).This IPA of 1: 1: DC245 solution by 0.2 μ m syringe filter to remove contaminant particles (for example dust).Sample is arranged on 70% the little recessed tissue culture of glass rotator by use and mixed (with the break-up shot gonosome) about 5 days then.

Next step uses the Horiba LA-910 of equipment fraction unit catcher and magnetic stirring bar that sample is measured.Prepare only to contain 1: 1 IPA of 30 grams: the independent sample of DC245 solution is as blank.Before measurement, place sample that branch such as 10ml prepares in bottle and allow 30 minutes (isolating big condensation product) of precipitation.Stirred in the measuring process, be set at 25 seconds sample time, use the 1.06-0.00i relative index of refraction with volume basis record data.Necessarily, sample further is that 1: 1 IPA: DC245 dilution is to reach the concentration within the HoribaLA-910 working range with ratio.In the workbook of Horiba LA-910, more detailed description is arranged, by being introduced in Insert Here.This operation is in addition at United States Patent (USP) 5,998,542 and United States Patent (USP) 5,929,162 in statement is arranged, be introduced in Insert Here by both complete.

The hardness number test

Among the present invention, term " product hardness " has reflected under following test condition and an ear of maize to be moved the distance of defined and to shift to required how much power in the cosmetic composition with controllable rate.The high more explanation product of this value is hard more, and the low more explanation product of value is soft more.This numerical value is at 27 ℃, 15% relative humidity, uses TA-XT2i texture analysis instrument to measure, said texture analysis instrument obtain from Texture Technology Corp. (Scarsdale, New York, USA).In the present invention, the product hardness value representation moves past the stainless steel bar of a long diameter 0.254mm of 16mm the amount of the needed power of compositions 12.2mm distance with the speed of 0.85mm/ second.This rod is linked to each other with instrument by suitable jointer (for example, drilling hole type chuck).Other test parameter comprises: speed 0.85mm/s before the test, test back speed 1.70mm/s triggers apart from 0.1mm.The operator's manual of the visible TA-XT2i of more details of instrument is incorporated herein by reference.

Correlation technique

The applicant has been found that in multiple purpose and is that compositions of the present invention is useful in the application of facilitation of mammal skin.Introduce and the application process of claimed compositions includes but not limited to: the 1) method of the affinity of increase cosmetics on skin at this; 2) method of increase moisture of skin; 3) improve the method for skin natural look; 4) the coating colour cosmetic is to the method for skin; 5) prevent, hinder and/or handle the method for wrinkle; 6) skin is provided the method for UV protection; 7) prevent, hinder and/or control the method for cunning outward appearance; 8) improve the method for dermal sensation and quality; 9) provide the method for uniform skin color; 10) prevent, hinder and/or handle spider shape blood vessel and cirsoid appearance; 11) cover the method for hair outward appearance on the skin; 12) defective and/or the flaw on the hidden application on human skin comprises that acne, senile plaque, freckle, melanotic nevus, cicatrix, eye pouch, birthmark, postinflammatory pigment are calm excessive or the like.The compositions that relates to prescription in each method of this discussion is topically applied to skin.

Following examples will more fully illustrate embodiment of the present invention.Except as otherwise noted, description and claims state book all umbers, percent and ratio all by weight.

Embodiment

Cosmetic product in the following example is for example understood the specific embodiments of cosmetic composition of the present invention, but the present invention is not limited to this.Those skilled in the art can make other improvement under the prerequisite that does not deviate from essence of the present invention and scope.The compositions of all illustrative can prepare by routine preparation and hybrid technology.The amount of component is listed by weight percentage and can not comprised less important material, as diluent, filler or the like.Therefore, listed preparation contains the listed component less important material relevant with any component therewith.

Example I

Be prepared as follows lip composition of the present invention:

Composition

Brazil wax 1.50

Ceresine 5.50

Candelilla wax 4.00

Hydrogenated vegetable oil 8.50

Acetylated lanolin 4.00

Propyl p-hydroxybenzoate 0.10

Castor oil acid cetyl 10.00

Ascorbic palmitate 1.00

Polybutene 2.00

Polysiloxane copolymer ¹

Stearyl dimethicone 5.97

(DC?2503?Cosmetic?wax)

Anhydrous lanolin 5.97

KSG 21 ²Elastomer gel 2.95

GE SFE 839 elastomer gels ³20.00

The associative structure phase

Lecithin 5.00

Nicotiamide 2.50

Pantothenylol 1.00

Glycerol 4.04

Pigment 9.00

Water 6.00

¹#1154-141-1, GE Silicones provides

²Be present in the 25% polydimethylsiloxane/copolyol cross linked polymer in the polydimethylsiloxane.

³Be stored in 5% dimethicone/vinyl dimethicone crosspolymers (mean diameter is less than 20 microns) in the annular dimethyl polysiloxane

The composition that is used for the associative structure phase except the pigment is mixed, until forming associative structure.After forming associative structure, add pigment and on the three-roller type grinder, grind.Then this mixture is mixed with all the other compositions, and be mixed to till the homogeneous mixture.(perhaps, add said components and being mixed together simultaneously.) with in the mould under this mixture heated to 85 ℃ impouring room temperature then.

With this lip pomade coating lip, be used to provide color, humidification and improvement lip sensation.

Example II

Be prepared as follows mascara of the present invention:

Composition Wt.%

Brazil wax 3.00

Glyceryl monostearate ¹7.50

White beeswax 3.75

The C18-C36 triglyceride ²5.50

The hydrogenating glycerol rosinate ³0.15

Propyl p-hydroxybenzoate 0.10

Paraffin 1,18/,125 2.25

Paraffin 2.25

Elastomer gel (KSG21) ⁴2.31

The DC9040 elastomer gel ⁷15.00

Lecithin ⁵2.25

Stearic acid 3X 4.00

Oleic acid 0.75

Triethanolamine 1.25

The cetyl potassium phosphate ⁶1.00

Lac, NF 3.00

Triethanolamine 0.47

EDTA trisodium 0.10

Black iron oxide 7.00

Polydimethylsiloxane (Simethicone) 0.20

Methyl parahydroxybenzoate 0.20

Ethylparaben 0.15

Phenyl phenol 0.80

Ethanol 40B, 190 checkings 4.00

Diazolidinyl urea 0.20

Deionized water 30.22

Dl-pantothenylol 0.35

Nicotiamide 2.25

Amount to 100.00

¹Can obtain from Henkel/Emery-by Emerest 2400

²Inc. can be obtained from Croda by Syncrowax HGL-C

³Inc.-can be obtained from Hercules by Foral 105

⁴Be present in the 25% polydimethylsiloxane/copolyol cross linked polymer in the polydimethylsiloxane

⁵Can obtain from Central Soya, Inc.-by Centrolex F

⁶Can obtain from Givaudan by Amphisol K

⁷Be present in 12% dimethicone/vinyl dimethicone crosspolymers (mean diameter is less than 20 microns) in the annular dimethyl polysiloxane

Wax and fat are mixed in being equipped with the container tank of heating source.With wax and fat heating and use conventional whisk mixed on low speed, so that make mixture liquefaction.Continue to mix until mix homogeneously.Add pigment to this homogeneous mixture.Increase mixing rate to high-grade and make pigment be mixed in the mixture about 30-35 minute, until homodisperse.Lasting mixing adds emulsifying agent simultaneously.

In second container tank that is equipped with heating source, add entry, add nicotiamide, lecithin and any other water dispersible property component subsequently.With this mixture heated and be mixed to about 80-95 ℃.If necessary add additional water to remedy the loss of water.

With aqueous mixture and merging of lipophilic mixture and the mixing of use dispersion type blender.Continue to mix and be cooled to about 65-70 ℃ until mixture.Add elastomer gel and antiseptic while mixing, allow mixture further to be cooled to 45-47 ℃.Add any remaining component while mixing.The mixture that merges is cooled to the temperature that is higher than solidification point, then in the container that impouring suits.

With this mascara composition coating eyelashes and/or eyebrow, be used to provide softness, humidification and opsonic action.

EXAMPLE III

Be prepared as follows humidification of the present invention with revealing liquid:

Component Wt%

Annular dimethyl polysiloxane (DC245) 17.35

The DC9040 elastomer gel ²18.00

Elastomer gel (KSG21) ¹18.33

Propyl p-hydroxybenzoate 0.20

Ethylene/acrylic acid copolymer microsphere 10.00

(Flobeads?EA?209，Kobo?Products

Inc. provide)

Glycerol 25.00

Water 8.00

Nicotiamide 3.00

Methyl parahydroxybenzoate 0.12

Amount to 100.00

¹Be present in the 25% polydimethylsiloxane/copolyol cross linked polymer in the polydimethylsiloxane

²Be stored in 12% dimethicone/vinyl dimethicone crosspolymers (mean diameter is less than 20 microns) in the annular dimethyl polysiloxane

In suitable rustless steel container jar, add annular dimethyl polysiloxane, DC9040, KSG21 and propyl p-hydroxybenzoate, till using conventional hybrid technology mixing simultaneously and being mixed to evenly.In another container tank, use conventional hybrid technology that nicotiamide and water are mixed to evenly.Next add glycerol, ethylene/acrylic acid copolymer microsphere and methyl parahydroxybenzoate to this nicotinamide soln, mix simultaneously until evenly.Next, this nicotiamide mixture and annular dimethyl polysiloxane mixture are merged and use conventional hybrid technology to mix until evenly.In then that the mixture impouring of this merging is the suitable container.

This humidification applied some make up reveal liquid coating face and/or health, be used to provide softness, humidification and opsonic action.

EXAMPLE IV

Be prepared as follows liquid foundation of the present invention:

Composition Wt%

Annular dimethyl polysiloxane 11.62

Dimethicone copolyol emulsifying agent 0.70

The KSG32 elastomer gel ¹5.38

GE SFE 839 elastomer gels ²10.00

Isononyl isononanoate 5.00

N-pro-pyl-4-hydroxy benzoic acid 0.20

Tridecandioic acid ethyl 0.03

Titanium dioxide 17.8

Yellow iron oxide 1.70

Red iron oxide 0.19

Black iron oxide 0.11

Methyl parahydroxybenzoate 0.12

Glycerol 10.00

2-amino-2-methyl-1-propanol 0.10

Water 36.45

Sucrose oleate 0.60

100.00

¹Be present in the 25%% lauryl polydimethylsiloxane/copolyol cross linked polymer in the Fancol ID

²Be stored in 5% dimethicone/vinyl dimethicone crosspolymers (mean diameter is less than 20 microns) in the annular dimethyl polysiloxane

In suitable rustless steel container jar, add annular dimethyl polysiloxane, dimethicone copolyol, GE SFE 839, KSG32, isononyl isononanoate, n-pro-pyl-4-hydroxy benzoic acid and tridecandioic acid ethyl, till using conventional hybrid technology mixing simultaneously and being mixed to evenly.Be equipped with in the container tank of heating source at another, sucrose oleate and water are heated to 50 ℃ and use conventional hybrid technology to be mixed to evenly.Allow this sucrose oleate mixture to be cooled to room temperature then.After the cooling, titanium dioxide, ferrum oxide, methyl parahydroxybenzoate, glycerol and 2-amino-2-methyl-1-propanol are added in this sucrose oleate mixture, mix simultaneously and form homogeneous pigment slurry, next, this sucrose oleate mixture and annular dimethyl polysiloxane mixture are merged, and use conventional hybrid technology to mix until evenly.In then that the mixture impouring of this merging is the suitable container.

This liquid foundation coating is facial, be used to provide softness, humidification and opsonic action.

EXAMPLE V

The preparation of product of minimizing microgroove of improving skin quality outward appearance is as follows:

Composition	Wt％
Composition	Wt％	DC9040 cross-linked elastomer gel ¹	50.25
Elastomer gel (KSG 21) ²	5.00	DC9040 cross-linked elastomer gel ¹	50.25
Elastomer gel (KSG 21) ²	5.00	Cyclohexyl methyl polysiloxanes (DC245)	10.00
Silicon dioxide, titanium dioxide, ferrum oxide (Ronasphere LDP)	8.00	Cyclohexyl methyl polysiloxanes (DC245)	10.00
	8.00	Isoeicosane (Permethyl102A)	5.00
Alkyl methyl polysiloxanes (DC AMS C30 wax)	1.50	Isoeicosane (Permethyl102A)	5.00
Alkyl methyl polysiloxanes (DC AMS C30 wax)	1.50	Propyl p-hydroxybenzoate	0.25
Tocopherol acetas	0.50	Propyl p-hydroxybenzoate	0.25
Tocopherol acetas	0.50	Water	9.35
Glycerol	7.00	Water	9.35
Glycerol	7.00	Nicotiamide	2.00
Panthenol	0.50	Nicotiamide	2.00
Panthenol	0.50	Dehydro sodium acetate	0.30
The EDTA disodium	0.10	Dehydro sodium acetate	0.30
The EDTA disodium	0.10	Phenoxyethanol	0.25

¹Contain 12% dimethyl polysiloxane/vinyl-dimethyl polysiloxanes cross linked polymer (mean diameter is less than 20 microns) in the cyclohexyl methyl polysiloxanes

²Contain 25% dimethyl polysiloxane/copolyol cross linked polymer in the dimethyl polysiloxane

In suitable container, add water, glycerol, nicotiamide, panthenol, dehydroacetic acid ester sodium, EDTA disodium and phenoxyethanol.By common process they are stirred until the water that obtains homogeneous.

In the other container that is equipped with thermal source, under slight stirring, add AMS wax and Permethyl and be heated to 75 ℃.In the 3rd container, under slight stirring, add Ronasphere and cyclohexyl methyl polysiloxanes (DC245) to form the Ronasphere/DC245 premix.In case wax/Permethyl mixture fully melts, in this mixture, add DC9040 and KSG21 elastomer and stir until evenly.Be cooled in the process of room temperature at wax/Permethyl/ elastomer blends, use Heidolph suspention agitator (#RZR50 type) or coordinate this mixture to be mixed with low speed (about 50-100 rev/min).In case wax/Permethyl/ elastomer blends is cooled to room temperature, add Ronasphere/DC245 premix and propyl p-hydroxybenzoate and tocopherol acetas, use Turrax T25 this mixture to be milled until even to form slight painted phase with low speed (about 8000 rev/mins).

Next step, mixed transparent water and form and aspect are arranged and use Turrax T25 it to be milled with low speed (about 8000 rev/mins), until water fully in conjunction with and form emulsion.Then the compositions that forms is put into suitable packing.

Example VI

Liquid foundation preparation of product of the present invention is as follows:

Composition	Wt％
Composition	Wt％	DC9040 cross-linked elastomer gel	46.25
Elastomer gel (KSG 21) ²	5.00	DC9040 cross-linked elastomer gel	46.25
Elastomer gel (KSG 21) ²	5.00	Cyclohexyl methyl polysiloxanes (DC245)	10.00
Ferrum oxide-polysiloxanes coating	4.00	Cyclohexyl methyl polysiloxanes (DC245)	10.00
Ferrum oxide-polysiloxanes coating	4.00	Titanium dioxide-polysiloxanes coating	8.00
Propyl p-hydroxybenzoate	0.25	Titanium dioxide-polysiloxanes coating	8.00
Propyl p-hydroxybenzoate	0.25	Tocopherol acetas	0.50
Isoeicosane (Permethyl 102A)	5.00	Tocopherol acetas	0.50
Isoeicosane (Permethyl 102A)	5.00	Alkyl methyl polysiloxanes (DC AMS C30 wax)	1.50
Water	9.35	Alkyl methyl polysiloxanes (DC AMS C30 wax)	1.50

Glycerol	7.00
Glycerol	7.00	Nicotiamide	2.00
Panthenol	0.50	Nicotiamide	2.00
Panthenol	0.50	Dehydro sodium acetate	0.30
The EDTA disodium	0.10	Dehydro sodium acetate	0.30
The EDTA disodium	0.10	Phenoxyethanol	0.25

¹12% dimethyl polysiloxane in the cyclohexyl methyl polysiloxanes/vinyl-dimethyl polysiloxanes cross linked polymer (mean diameter is less than 20 microns)

²25% dimethyl polysiloxane in the dimethyl polysiloxane/copolyol cross linked polymer

In suitable container, add water, glycerol, nicotiamide, panthenol, dehydro sodium acetate, EDTA disodium and phenoxyethanol.By common process they are stirred until obtaining transparent water.

In other container, under slight stirring, add AMS wax and Permethyl and be heated to 75 ℃.In the 3rd container, interpolation ferrum oxide, titanium dioxide and cyclohexyl methyl polysiloxanes (DC245) also grind under high shear (about 20,000 units) so that pigment is separated reunion, to form ferrum oxide/titanium dioxide/DC245 premix.In case wax/Permethyl mixture fully melts, in this mixture, add DC9040 and KSG21 elastomer and stir until evenly.Be cooled in the process of room temperature at wax/Permethyl/ elastomer blends, use Heidolph suspention agitator (#RZR50 type) or coordinate this mixture to be mixed with low speed (about 50-100 rev/min).In case wax/Permethyl/ elastomer blends is cooled to room temperature, add ferrum oxide/titanium dioxide/DC245 premix and propyl p-hydroxybenzoate and tocopherol acetas, use Turrax T25 this mixture to be milled until evenly to be formed with form and aspect with low speed (about 8000 rev/mins).

Example VII A

Composition	Wt％
Composition	Wt％	DC9040 cross-linked elastomer gel ¹	50.25
Elastomer gel (KSG 21) ²	5.00	DC9040 cross-linked elastomer gel ¹	50.25
Elastomer gel (KSG 21) ²	5.00	Cyclohexyl methyl polysiloxanes (DC245)	10.00
Ethylene acrylate copolymer (EA209)	8.00	Cyclohexyl methyl polysiloxanes (DC245)	10.00
Ethylene acrylate copolymer (EA209)	8.00	Isoeicosane (Permethyl 102A)	5.00
Alkyl methyl polysiloxanes (DC AMS C30 wax)	1.50	Isoeicosane (Permethyl 102A)	5.00
Alkyl methyl polysiloxanes (DC AMS C30 wax)	1.50	Propyl p-hydroxybenzoate	0.25
Tocopherol acetas	0.50	Propyl p-hydroxybenzoate	0.25
Tocopherol acetas	0.50	Water	9.35
Glycerol	7.00	Water	9.35
Glycerol	7.00	Nicotiamide	2.00
Panthenol	0.50	Nicotiamide	2.00
Panthenol	0.50	Dehydro sodium acetate	0.30
The EDTA disodium	0.10	Dehydro sodium acetate	0.30
The EDTA disodium	0.10	Phenoxyethanol	0.25

In the other container that is equipped with thermal source, under slight stirring, add AMS wax and Permethyl and be heated to 75 ℃.In the 3rd container, under slight stirring, add EA209 and cyclohexyl methyl polysiloxanes (DC245) to form the EA209/DC245 premix.In case wax/Permethyl mixture fully melts, in this mixture, add DC9040 and KSG21 elastomer and stir until evenly.Be cooled in the process of room temperature at wax/Permethyl/ elastomer blends, use Heidolph suspention agitator (#RzR50 type) or coordinate this mixture to be mixed with low speed (about 50-100 rev/min).In case wax/Permethyl/ elastomer blends is cooled to room temperature, add EA209/DC245 premix and propyl p-hydroxybenzoate and tocopherol acetas, use Turrax T25 this mixture to be milled until evenly to be formed with form and aspect with low speed (about 8000 rev/mins).

Example VII A I-IX

Make and suitablely to be coated on facial vanishing cream in order to provide softening to skin, to moisturize, regulate and effectively reduce the outward appearance of cunning/bright skin.

	?? VIII	??? IX
	?? VIII	??? IX	Composition	?? Wt％	?? Wt％
The cyclohexyl methyl polysiloxanes	???29.00	???31.00	Composition	?? Wt％	?? Wt％
The cyclohexyl methyl polysiloxanes	???29.00	???31.00	The DC9040 silicone elastomer gel	???17.50	???17.50
Ethylene/acrylic acid copolymer microsphere (the Flobeads EA 209 that Kobo Products company provides)	???10.00	???10.00	The DC9040 silicone elastomer gel	???17.50	???17.50
	???10.00	???10.00	Silicon dioxide and titanium dioxide and ferrum oxide (Ronasphere LDP)	???10.00	????-
Allyl methacrylate copolymer (Polypore L200)	???2.00	????-		???10.00	????-
Allyl methacrylate copolymer (Polypore L200)	???2.00	????-	Aluminium-magnesium silicate (Sebumase)	???-	???5.00
Silicon dioxide	???-	???5.00	Aluminium-magnesium silicate (Sebumase)	???-	???5.00
Silicon dioxide	???-	???5.00	The KSG21 elastomer gel	???2.50	???2.50

Water	??15.00	??15.00
Water	??15.00	??15.00	Glycerol	??10.00	??10.00
Nicotiamide	??3.50	??3.50	Glycerol	??10.00	??10.00
Nicotiamide	??3.50	??3.50	Antiseptic	??0.50	??0.50
Amount to	??100.00	??100.00	Antiseptic	??0.50	??0.50

In suitable container, hybrid ring methyl polysiloxane and KSG21, mixing is in order to dispersed polymeres under high shear.The material of mixed together and water compatible and mixing in other container until transparent.Under high shear, mix in order to emulsifying mixt.Add silicone elastomer gel and mix until evenly.Add surplus materials and mix until evenly.

Embodiment X-XII

Make the suitable vanishing cream of face that is coated in order to effect that provides long-acting to skin, softens, moisturizes, regulates and the outward appearance that reduces cunning/bright skin.

	Phase	??X	??XI	??XII
	Phase	??X	??XI	??XII	Composition		? Wt％	? Wt％	? Wt％
Non-emulsifying elastomer gel (DC9040)	????A	??40	??25	??30	Composition		? Wt％	? Wt％	? Wt％
Non-emulsifying elastomer gel (DC9040)	????A	??40	??25	??30	Encircle five polysiloxanes	????A	??20	??34	??14
Emulsifying elastomer gel (KSG21)	????A	??5	??5	??5	Encircle five polysiloxanes	????A	??20	??34	??14
Emulsifying elastomer gel (KSG21)	????A	??5	??5	??5	Microgranule
The allyl methacrylate cross linked polymer		??-	??-	??1.5	Microgranule
The allyl methacrylate cross linked polymer		??-	??-	??1.5	Treated powder ^*		??11	??12	??12.5
Film former					Treated powder ^*		??11	??12	??12.5
Film former					Polysiloxanes 7 (siloxanes addition polymerization compound SA70)		??-	??-	??17
Firming agent							??-	??-	??17
Firming agent					Hard ester group dimethyl polysiloxane		??-	??3	??-

Water
Water				Deionized water	????9	????10	????16
Glycerol	????10	????10	????3	Deionized water	????9	????10	????16
Glycerol	????10	????10	????3	Antiseptic	????1	????1	????1
Sunscreen	????4	????-	????-	Antiseptic	????1	????1	????1

^*The mixture of=ferrum oxide and titanium dioxide

In suitable rustless steel container, mix the A phase component until evenly.In the other vessel in heating aqueous phase substance to 50 ℃ of equipment thermal source and mix until evenly.Add sunscreen material, antiseptic, film former and microgranule batch of material and mix until evenly.If the use firming agent, heating ring five polysiloxane mixtures melt needed temperature and add firming agent to firming agent.

Cooling water and polysiloxanes are mutually to be lower than 30 ℃ and mix and then the formation emulsion under high shear.

Embodiment XIII-XIV

Liquid foundation cream of the present invention is produced as follows.

XIII

??? Phase	?????? Composition	??? Wt％
??? Phase	?????? Composition	??? Wt％	????A	???X-21-507	???12.50
????A	???KSG-15	???37.50	????A	???X-21-507	???12.50
????A	???KSG-15	???37.50	????A	Propyl parabene	???0.20
????A	Isononyl isononanoate	???7.00	????A	Propyl parabene	???0.20
????A	Isononyl isononanoate	???7.00	????A	???SAT-TR-77891	???8.97
????A	???DHL-Y-77492	???0.86	????A	???SAT-TR-77891	???8.97
????A	???DHL-Y-77492	???0.86	????A	???DHL-R-77491	???0.12
????A	???DHL-B-77499	???0.05	????A	???DHL-R-77491	???0.12
????A	???DHL-B-77499	???0.05	????B	Nipagin	???0.12
????B	???Polyderm?PE/PA	???13.00	????B	Nipagin	???0.12

????B	Glycerol	????6.07
????B	Glycerol	????6.07	????B	?AMP95	????0.14
????B	?SMO	????0.60	????B	?AMP95	????0.14
????B	?SMO	????0.60	????B	Water	????12.87
		????100.00	????B	Water	????12.87

XIV

? Phase	???????????? Composition	??? Wt％
? Phase	???????????? Composition	??? Wt％	??A	KSG-15	??33.00
??A	KSG-21	??11.00	??A	KSG-15	??33.00
??A	KSG-21	??11.00	??A	Isononyl isononanoate	??6.16
??B	GLW75AMPC (74.75%TiO2,12.5% water, 12.5% glycerol, 0.25%AMP)	??10.55	??A	Isononyl isononanoate	??6.16
??B		??10.55	??B	GLW45YAMP (45%Fe2O3,28.46% water, 26.30% glycerol, 0.24%AMP)	??1.68
??B	GLW55RAMP (55%Fe2O3,23.25% water, 21.50% glycerol, 0.25%AMP)	??0.20	??B		??1.68
??B		??0.20	??B	GLW60BAMP (60%Fe2O3,21.67% water, 19.80% glycerol, 0.25%AMP)	??0.08
??B	Polvderm?PE/PA	??12.10	??B		??0.08
??B	Polvderm?PE/PA	??12.10	??B	AMP95	??0.09
??B	Glycerol	??3.53	??B	AMP95	??0.09
??B	Glycerol	??3.53	??B	Water	??21.08
??B	SMO (O-1570 Ryoto sugar ester)	??0.53	??B	Water	??21.08
??B	SMO (O-1570 Ryoto sugar ester)	??0.53		Amount to	??100.00

Every kind of composition is combined in the component that contains pigment and mixes down and disperseed until composition in 30 minutes at 5000 rev/mins.Every kind of composition be combined in do not contain pigment mutually in and mix down until evenly (approximately 10-15 minute) at maximum 1300 rev/mins.Slowly water being added to siloxanes mixes fully until emulsion in mutually.Finish in case mix, mixture is poured in the suitable container also stored in order to using.

Embodiment XV-XIX

Liquid foundation is prepared as follows:

Composition	? Phase	?? Wt％	?? Wt％	?? Wt％	?? Wt％	?? Wt％
Composition	? Phase	?? Wt％	?? Wt％	?? Wt％	?? Wt％	?? Wt％	Encircle five polysiloxanes	??A	??21.64	??33.64	??18.14	??12.75	??14.30
The DC9040 silicone elastomer gel	??A	??40.00	??25.00	??40.00	??30.00	??30.00	Encircle five polysiloxanes	??A	??21.64	??33.64	??18.14	??12.75	??14.30
The DC9040 silicone elastomer gel	??A	??40.00	??25.00	??40.00	??30.00	??30.00	The KSG-21 elastomer gel	??A	??5.00	??5.00	??5.00	??5.00	??5.00
Polysiloxanes-7	??B	??0.00	??0.00	??0.00	??17.39	??17.39	The KSG-21 elastomer gel	??A	??5.00	??5.00	??5.00	??5.00	??5.00
Polysiloxanes-7	??B	??0.00	??0.00	??0.00	??17.39	??17.39	The allyl methacrylate cross linked polymer	??B	??0.00	??0.00	??0.00	??1.50	??1.50
The stearyl dimethicone		??0.00	??3.00	??0.00	??0.00	??0.00	The allyl methacrylate cross linked polymer	??B	??0.00	??0.00	??0.00	??1.50	??1.50
The stearyl dimethicone		??0.00	??3.00	??0.00	??0.00	??0.00	Titanium dioxide ﹠ mineral oil ﹠ methyl polysiloxane	??A	??9.90	??9.90	??9.90	??9.90	??0.00
Titanium dioxide and triethyl group caprylyl silane	??A	??0.00	??0.00	??0.00	??0.00	??8.25	Titanium dioxide ﹠ mineral oil ﹠ methyl polysiloxane	??A	??9.90	??9.90	??9.90	??9.90	??0.00
Titanium dioxide and triethyl group caprylyl silane	??A	??0.00	??0.00	??0.00	??0.00	??8.25	Antiseptic	??B	??0.30	??0.30	??0.30	??0.30	??0.30
Pigment	??A	??3.16	??3.16	??3.16	??3.16	??3.26	Antiseptic	??B	??0.30	??0.30	??0.30	??0.30	??0.30
Pigment	??A	??3.16	??3.16	??3.16	??3.16	??3.26	PAROSOL 1789	??B	??0.00	??0.00	??1.00	??0.00	??0.00
The octyl group salicylate	??B	??0.00	??0.00	??2.00	??0.00	??0.00	PAROSOL 1789	??B	??0.00	??0.00	??1.00	??0.00	??0.00
The octyl group salicylate	??B	??0.00	??0.00	??2.00	??0.00	??0.00	Octocrilene	??B	??0.00	??0.00	??0.50	??0.00	??0.00
							Octocrilene	??B	??0.00	??0.00	??0.50	??0.00	??0.00
							Water		??9.55	??9.55	??8.33	??16.55	??16.55
Phenylbenzimidazolesulfonic acid		??0.00	??0.00	??0.60	??0.00	??0.00	Water		??9.55	??9.55	??8.33	??16.55	??16.55

Triethanolamine	??0.00	??0.00	??0.62	??0.00	??0.00
Triethanolamine	??0.00	??0.00	??0.62	??0.00	??0.00	Glycerol	??10.00	??10.00	??10.00	??3.00	??3.00
Nipagin	??0.10	??0.10	??0.10	??0.10	??0.10	Glycerol	??10.00	??10.00	??10.00	??3.00	??3.00
Nipagin	??0.10	??0.10	??0.10	??0.10	??0.10	The EDTA disodium	??0.10	??0.10	??0.10	??0.10	??0.10
Benzyl alcohol	??0.25	??0.25	??0.25	??0.25	??0.25	The EDTA disodium	??0.10	??0.10	??0.10	??0.10	??0.10

In suitable rustless steel container made, mix the A phase component until evenly.In the container of other equipment thermal source, heating aqueous phase substance to 50 ℃ and mixing until evenly.Add sunscreen material, antiseptic, film former and microgranule (B mutually) batch of material and mix until evenly.If the use firming agent, heating ring five polysiloxane mixtures melt needed temperature and add firming agent to firming agent.

Claims

1. cosmetic composition is characterized in that comprising:

(i) non-emulsifying cross-linked siloxane elastomer, content are from about 0.1% to about 15%, and its mean diameter is less than 20 microns;

(ii) emulsifying cross-linked siloxane elastomer, content from about 0.1% to about 15%;

The (iii) solvent of crosslinked siloxane elastomer, content from about 10% to about 80%;

(iv) alternatively, skin conditioning agent, content from 0 to about 50%; With

(v) water, content is from greater than about 0 to about 95%.

2. the cosmetic composition of claim 1, wherein skin conditioning agent is selected from wetting agent, remover, emollient and composition thereof.

3. the cosmetic composition of claim 2, wherein skin conditioning agent is a wetting agent.

4. the cosmetic composition of claim 3, wherein wetting agent is selected from propylene glycol, dipropylene glycol, polypropylene glycol, Polyethylene Glycol, sorbitol, hydroxypropyl sorbitol, hexanediol, glycerol, 1,3-butanediol, 1,2,6-hexanetriol, ethoxylated glycerol, propoxylated glycerol and composition thereof.

5. the cosmetic composition of claim 1, wherein said composition comprises emulsifying agent in addition.

6. the cosmetic composition of claim 5, wherein emulsifying agent is the poly (oxyalkylene) base co-polymer.

7. the cosmetic composition of claim 1 comprises colorant in addition, and it is selected from inorganic pigment, organic pigment, color lake, dyestuff and toner.

8. the cosmetic composition of claim 7, wherein pigment is selected from Talcum, Muscovitum, magnesium carbonate, calcium carbonate, magnesium silicate, aluminium-magnesium silicate, silicon dioxide, titanium dioxide, zinc oxide, iron oxide red, iron oxide yellow, iron oxide black, ultramarine, nylon powder, polyethylene powder, methacrylate powder, polystyrene powder, silk powder, crystalline cellulose, starch, metatitanic acid Muscovitum, ferrum oxide metatitanic acid Muscovitum, bismuth oxychloride, Margarita, emerylite, coated interference pigment and composition thereof.

9. the cosmetic composition of claim 1, wherein the form of said composition is foundation cream, mascara, covers flaw agent, informer, eyebrow coloured silk, eye shadow, kermes, lip gloss or lip pomade.

10. the cosmetic composition of claim 1, wherein said composition comprises activating agent in addition, and it is selected from sunscreen actives agent, film former, gloss controlling agent and compositions thereof.